Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

Autores
The GR@ACE study group; Jansen, Iris E.; van der Lee, Sven J.; Gomez-Fonseca, Duber; de Rojas, Itziar; Dalmasso, Maria Carolina; Grenier Boley, Benjamin; Zettergren, Anna; Mishra, Aniket; Ali, Muhammad; Andrade, Victor; Bellenguez, Céline; Kleineidam, Luca; Küçükali, Fahri; Sung, Yun Ju; Tesí, Niccolo; Vromen, Ellen M.; Wightman, Douglas P.; Alcolea, Daniel; Alegret, Montserrat; Alvarez, Ignacio; Amouyel, Philippe; Athanasiu, Lavinia; Bahrami, Shahram; Bailly, Henri; Belbin, Olivia; Bergh, Sverre; Bertram, Lars; Biessels, Geert Jan; Blennow, Kaj
Año de publicación
2022
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Amyloid-beta 42 (Aβ42) and phosphorylated tau (pTau) levels in cerebrospinal fluid (CSF) reflect core features of the pathogenesis of Alzheimer’s disease (AD) more directly than clinical diagnosis. Initiated by the European Alzheimer & Dementia Biobank (EADB), the largest collaborative effort on genetics underlying CSF biomarkers was established, including 31 cohorts with a total of 13,116 individuals (discovery n = 8074; replication n = 5042 individuals). Besides the APOE locus, novel associations with two other well-established AD risk loci were observed; CR1 was shown a locus for Aβ42 and BIN1 for pTau. GMNC and C16orf95 were further identified as loci for pTau, of which the latter is novel. Clustering methods exploring the influence of all known AD risk loci on the CSF protein levels, revealed 4 biological categories suggesting multiple Aβ42 and pTau related biological pathways involved in the etiology of AD. In functional follow-up analyses, GMNC and C16orf95 both associated with lateral ventricular volume, implying an overlap in genetic etiology for tau levels and brain ventricular volume.
Fil: The GR@ACE study group. No especifíca;
Fil: Jansen, Iris E.. Amsterdam Neuroscience; Países Bajos. Vrije Universiteit Amsterdam; Países Bajos
Fil: van der Lee, Sven J.. Vrije Universiteit Amsterdam; Países Bajos. Amsterdam Neuroscience; Países Bajos
Fil: Gomez-Fonseca, Duber. Washington University School Of Medicine In St. Louis; Estados Unidos
Fil: de Rojas, Itziar. Universitat Internacional de Catalunya; España. Centro de Investigación Biomédica En Red de Enfermedades Neurodegenerativas; España
Fil: Dalmasso, Maria Carolina. Universidad Nacional Arturo Jauretche. Unidad Ejecutora de Estudios en Neurociencias y Sistemas Complejos. Provincia de Buenos Aires. Ministerio de Salud. Hospital Alta Complejidad en Red El Cruce Dr. Néstor Carlos Kirchner Samic. Unidad Ejecutora de Estudios en Neurociencias y Sistemas Complejos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Unidad Ejecutora de Estudios en Neurociencias y Sistemas Complejos; Argentina. University of Cologne; Alemania
Fil: Grenier Boley, Benjamin. Institut Pasteur de Lille; Francia
Fil: Zettergren, Anna. University of Gothenburg; Suecia
Fil: Mishra, Aniket. Université de Bordeaux; Francia
Fil: Ali, Muhammad. Washington University School Of Medicine In St. Louis; Estados Unidos
Fil: Andrade, Victor. Universitat Bonn; Alemania. University of Cologne; Alemania
Fil: Bellenguez, Céline. Institut Pasteur de Lille; Francia
Fil: Kleineidam, Luca. German Center for Neurodegenerative Diseases; Alemania. University of Cologne; Alemania. Universitat Bonn; Alemania
Fil: Küçükali, Fahri. VIB Center for Molecular Neurology; Bélgica. Universiteit Antwerp; Bélgica
Fil: Sung, Yun Ju. Washington University School Of Medicine In St. Louis; Estados Unidos
Fil: Tesí, Niccolo. Amsterdam Neuroscience; Países Bajos. Vrije Universiteit Amsterdam; Países Bajos
Fil: Vromen, Ellen M.. Vrije Universiteit Amsterdam; Países Bajos. Amsterdam Neuroscience; Países Bajos
Fil: Wightman, Douglas P.. Vrije Universiteit Amsterdam; Países Bajos
Fil: Alcolea, Daniel. Centro de Investigación Biomédica En Red de Enfermedades Neurodegenerativas; España. Universitat Autònoma de Barcelona; España
Fil: Alegret, Montserrat. Universitat Internacional de Catalunya; España. Centro de Investigación Biomédica En Red de Enfermedades Neurodegenerativas; España
Fil: Alvarez, Ignacio. Hospital Universitari Mutua de Terrassa; España. Fundació per a la Recerca Biomèdica i Social Mútua de Terrassa; España
Fil: Amouyel, Philippe. Institut Pasteur de Lille; Francia
Fil: Athanasiu, Lavinia. University of Oslo; Noruega
Fil: Bahrami, Shahram. University of Oslo; Noruega
Fil: Bailly, Henri. Université Paris Cité; Francia
Fil: Belbin, Olivia. Centro de Investigación Biomédica En Red de Enfermedades Neurodegenerativas; España. Universitat Autònoma de Barcelona; España
Fil: Bergh, Sverre. Vestfold Hospital Trust; Noruega. Innlandet Hospital Trust; Noruega
Fil: Bertram, Lars. Universität Zu Lübeck; Alemania
Fil: Biessels, Geert Jan. University of Utrecht; Países Bajos
Fil: Blennow, Kaj. University of Gothenburg; Suecia. Sahlgrenska University Hospital; Suecia
Materia
ALZHEIMER’S DISEASE
AMYLOID-BETA
CEREBROSPINAL FLUID
GWAS
TAU
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/215593

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network_name_str CONICET Digital (CONICET)
spelling Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkersThe GR@ACE study groupJansen, Iris E.van der Lee, Sven J.Gomez-Fonseca, Duberde Rojas, ItziarDalmasso, Maria CarolinaGrenier Boley, BenjaminZettergren, AnnaMishra, AniketAli, MuhammadAndrade, VictorBellenguez, CélineKleineidam, LucaKüçükali, FahriSung, Yun JuTesí, NiccoloVromen, Ellen M.Wightman, Douglas P.Alcolea, DanielAlegret, MontserratAlvarez, IgnacioAmouyel, PhilippeAthanasiu, LaviniaBahrami, ShahramBailly, HenriBelbin, OliviaBergh, SverreBertram, LarsBiessels, Geert JanBlennow, KajALZHEIMER’S DISEASEAMYLOID-BETACEREBROSPINAL FLUIDGWASTAUhttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3Amyloid-beta 42 (Aβ42) and phosphorylated tau (pTau) levels in cerebrospinal fluid (CSF) reflect core features of the pathogenesis of Alzheimer’s disease (AD) more directly than clinical diagnosis. Initiated by the European Alzheimer & Dementia Biobank (EADB), the largest collaborative effort on genetics underlying CSF biomarkers was established, including 31 cohorts with a total of 13,116 individuals (discovery n = 8074; replication n = 5042 individuals). Besides the APOE locus, novel associations with two other well-established AD risk loci were observed; CR1 was shown a locus for Aβ42 and BIN1 for pTau. GMNC and C16orf95 were further identified as loci for pTau, of which the latter is novel. Clustering methods exploring the influence of all known AD risk loci on the CSF protein levels, revealed 4 biological categories suggesting multiple Aβ42 and pTau related biological pathways involved in the etiology of AD. In functional follow-up analyses, GMNC and C16orf95 both associated with lateral ventricular volume, implying an overlap in genetic etiology for tau levels and brain ventricular volume.Fil: The GR@ACE study group. No especifíca;Fil: Jansen, Iris E.. Amsterdam Neuroscience; Países Bajos. Vrije Universiteit Amsterdam; Países BajosFil: van der Lee, Sven J.. Vrije Universiteit Amsterdam; Países Bajos. Amsterdam Neuroscience; Países BajosFil: Gomez-Fonseca, Duber. Washington University School Of Medicine In St. Louis; Estados UnidosFil: de Rojas, Itziar. Universitat Internacional de Catalunya; España. Centro de Investigación Biomédica En Red de Enfermedades Neurodegenerativas; EspañaFil: Dalmasso, Maria Carolina. Universidad Nacional Arturo Jauretche. Unidad Ejecutora de Estudios en Neurociencias y Sistemas Complejos. Provincia de Buenos Aires. Ministerio de Salud. Hospital Alta Complejidad en Red El Cruce Dr. Néstor Carlos Kirchner Samic. Unidad Ejecutora de Estudios en Neurociencias y Sistemas Complejos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Unidad Ejecutora de Estudios en Neurociencias y Sistemas Complejos; Argentina. University of Cologne; AlemaniaFil: Grenier Boley, Benjamin. Institut Pasteur de Lille; FranciaFil: Zettergren, Anna. University of Gothenburg; SueciaFil: Mishra, Aniket. Université de Bordeaux; FranciaFil: Ali, Muhammad. Washington University School Of Medicine In St. Louis; Estados UnidosFil: Andrade, Victor. Universitat Bonn; Alemania. University of Cologne; AlemaniaFil: Bellenguez, Céline. Institut Pasteur de Lille; FranciaFil: Kleineidam, Luca. German Center for Neurodegenerative Diseases; Alemania. University of Cologne; Alemania. Universitat Bonn; AlemaniaFil: Küçükali, Fahri. VIB Center for Molecular Neurology; Bélgica. Universiteit Antwerp; BélgicaFil: Sung, Yun Ju. Washington University School Of Medicine In St. Louis; Estados UnidosFil: Tesí, Niccolo. Amsterdam Neuroscience; Países Bajos. Vrije Universiteit Amsterdam; Países BajosFil: Vromen, Ellen M.. Vrije Universiteit Amsterdam; Países Bajos. Amsterdam Neuroscience; Países BajosFil: Wightman, Douglas P.. Vrije Universiteit Amsterdam; Países BajosFil: Alcolea, Daniel. Centro de Investigación Biomédica En Red de Enfermedades Neurodegenerativas; España. Universitat Autònoma de Barcelona; EspañaFil: Alegret, Montserrat. Universitat Internacional de Catalunya; España. Centro de Investigación Biomédica En Red de Enfermedades Neurodegenerativas; EspañaFil: Alvarez, Ignacio. Hospital Universitari Mutua de Terrassa; España. Fundació per a la Recerca Biomèdica i Social Mútua de Terrassa; EspañaFil: Amouyel, Philippe. Institut Pasteur de Lille; FranciaFil: Athanasiu, Lavinia. University of Oslo; NoruegaFil: Bahrami, Shahram. University of Oslo; NoruegaFil: Bailly, Henri. Université Paris Cité; FranciaFil: Belbin, Olivia. Centro de Investigación Biomédica En Red de Enfermedades Neurodegenerativas; España. Universitat Autònoma de Barcelona; EspañaFil: Bergh, Sverre. Vestfold Hospital Trust; Noruega. Innlandet Hospital Trust; NoruegaFil: Bertram, Lars. Universität Zu Lübeck; AlemaniaFil: Biessels, Geert Jan. University of Utrecht; Países BajosFil: Blennow, Kaj. University of Gothenburg; Suecia. Sahlgrenska University Hospital; SueciaSpringer2022-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/215593The GR@ACE study group; Jansen, Iris E.; van der Lee, Sven J.; Gomez-Fonseca, Duber; de Rojas, Itziar; et al.; Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers; Springer; Acta Neuropathologica; 144; 5; 11-2022; 821-8420001-6322CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1007/s00401-022-02454-zinfo:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007/s00401-022-02454-zinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:07:48Zoai:ri.conicet.gov.ar:11336/215593instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:07:48.537CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers
title Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers
spellingShingle Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers
The GR@ACE study group
ALZHEIMER’S DISEASE
AMYLOID-BETA
CEREBROSPINAL FLUID
GWAS
TAU
title_short Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers
title_full Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers
title_fullStr Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers
title_full_unstemmed Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers
title_sort Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers
dc.creator.none.fl_str_mv The GR@ACE study group
Jansen, Iris E.
van der Lee, Sven J.
Gomez-Fonseca, Duber
de Rojas, Itziar
Dalmasso, Maria Carolina
Grenier Boley, Benjamin
Zettergren, Anna
Mishra, Aniket
Ali, Muhammad
Andrade, Victor
Bellenguez, Céline
Kleineidam, Luca
Küçükali, Fahri
Sung, Yun Ju
Tesí, Niccolo
Vromen, Ellen M.
Wightman, Douglas P.
Alcolea, Daniel
Alegret, Montserrat
Alvarez, Ignacio
Amouyel, Philippe
Athanasiu, Lavinia
Bahrami, Shahram
Bailly, Henri
Belbin, Olivia
Bergh, Sverre
Bertram, Lars
Biessels, Geert Jan
Blennow, Kaj
author The GR@ACE study group
author_facet The GR@ACE study group
Jansen, Iris E.
van der Lee, Sven J.
Gomez-Fonseca, Duber
de Rojas, Itziar
Dalmasso, Maria Carolina
Grenier Boley, Benjamin
Zettergren, Anna
Mishra, Aniket
Ali, Muhammad
Andrade, Victor
Bellenguez, Céline
Kleineidam, Luca
Küçükali, Fahri
Sung, Yun Ju
Tesí, Niccolo
Vromen, Ellen M.
Wightman, Douglas P.
Alcolea, Daniel
Alegret, Montserrat
Alvarez, Ignacio
Amouyel, Philippe
Athanasiu, Lavinia
Bahrami, Shahram
Bailly, Henri
Belbin, Olivia
Bergh, Sverre
Bertram, Lars
Biessels, Geert Jan
Blennow, Kaj
author_role author
author2 Jansen, Iris E.
van der Lee, Sven J.
Gomez-Fonseca, Duber
de Rojas, Itziar
Dalmasso, Maria Carolina
Grenier Boley, Benjamin
Zettergren, Anna
Mishra, Aniket
Ali, Muhammad
Andrade, Victor
Bellenguez, Céline
Kleineidam, Luca
Küçükali, Fahri
Sung, Yun Ju
Tesí, Niccolo
Vromen, Ellen M.
Wightman, Douglas P.
Alcolea, Daniel
Alegret, Montserrat
Alvarez, Ignacio
Amouyel, Philippe
Athanasiu, Lavinia
Bahrami, Shahram
Bailly, Henri
Belbin, Olivia
Bergh, Sverre
Bertram, Lars
Biessels, Geert Jan
Blennow, Kaj
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv ALZHEIMER’S DISEASE
AMYLOID-BETA
CEREBROSPINAL FLUID
GWAS
TAU
topic ALZHEIMER’S DISEASE
AMYLOID-BETA
CEREBROSPINAL FLUID
GWAS
TAU
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.1
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv Amyloid-beta 42 (Aβ42) and phosphorylated tau (pTau) levels in cerebrospinal fluid (CSF) reflect core features of the pathogenesis of Alzheimer’s disease (AD) more directly than clinical diagnosis. Initiated by the European Alzheimer & Dementia Biobank (EADB), the largest collaborative effort on genetics underlying CSF biomarkers was established, including 31 cohorts with a total of 13,116 individuals (discovery n = 8074; replication n = 5042 individuals). Besides the APOE locus, novel associations with two other well-established AD risk loci were observed; CR1 was shown a locus for Aβ42 and BIN1 for pTau. GMNC and C16orf95 were further identified as loci for pTau, of which the latter is novel. Clustering methods exploring the influence of all known AD risk loci on the CSF protein levels, revealed 4 biological categories suggesting multiple Aβ42 and pTau related biological pathways involved in the etiology of AD. In functional follow-up analyses, GMNC and C16orf95 both associated with lateral ventricular volume, implying an overlap in genetic etiology for tau levels and brain ventricular volume.
Fil: The GR@ACE study group. No especifíca;
Fil: Jansen, Iris E.. Amsterdam Neuroscience; Países Bajos. Vrije Universiteit Amsterdam; Países Bajos
Fil: van der Lee, Sven J.. Vrije Universiteit Amsterdam; Países Bajos. Amsterdam Neuroscience; Países Bajos
Fil: Gomez-Fonseca, Duber. Washington University School Of Medicine In St. Louis; Estados Unidos
Fil: de Rojas, Itziar. Universitat Internacional de Catalunya; España. Centro de Investigación Biomédica En Red de Enfermedades Neurodegenerativas; España
Fil: Dalmasso, Maria Carolina. Universidad Nacional Arturo Jauretche. Unidad Ejecutora de Estudios en Neurociencias y Sistemas Complejos. Provincia de Buenos Aires. Ministerio de Salud. Hospital Alta Complejidad en Red El Cruce Dr. Néstor Carlos Kirchner Samic. Unidad Ejecutora de Estudios en Neurociencias y Sistemas Complejos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Unidad Ejecutora de Estudios en Neurociencias y Sistemas Complejos; Argentina. University of Cologne; Alemania
Fil: Grenier Boley, Benjamin. Institut Pasteur de Lille; Francia
Fil: Zettergren, Anna. University of Gothenburg; Suecia
Fil: Mishra, Aniket. Université de Bordeaux; Francia
Fil: Ali, Muhammad. Washington University School Of Medicine In St. Louis; Estados Unidos
Fil: Andrade, Victor. Universitat Bonn; Alemania. University of Cologne; Alemania
Fil: Bellenguez, Céline. Institut Pasteur de Lille; Francia
Fil: Kleineidam, Luca. German Center for Neurodegenerative Diseases; Alemania. University of Cologne; Alemania. Universitat Bonn; Alemania
Fil: Küçükali, Fahri. VIB Center for Molecular Neurology; Bélgica. Universiteit Antwerp; Bélgica
Fil: Sung, Yun Ju. Washington University School Of Medicine In St. Louis; Estados Unidos
Fil: Tesí, Niccolo. Amsterdam Neuroscience; Países Bajos. Vrije Universiteit Amsterdam; Países Bajos
Fil: Vromen, Ellen M.. Vrije Universiteit Amsterdam; Países Bajos. Amsterdam Neuroscience; Países Bajos
Fil: Wightman, Douglas P.. Vrije Universiteit Amsterdam; Países Bajos
Fil: Alcolea, Daniel. Centro de Investigación Biomédica En Red de Enfermedades Neurodegenerativas; España. Universitat Autònoma de Barcelona; España
Fil: Alegret, Montserrat. Universitat Internacional de Catalunya; España. Centro de Investigación Biomédica En Red de Enfermedades Neurodegenerativas; España
Fil: Alvarez, Ignacio. Hospital Universitari Mutua de Terrassa; España. Fundació per a la Recerca Biomèdica i Social Mútua de Terrassa; España
Fil: Amouyel, Philippe. Institut Pasteur de Lille; Francia
Fil: Athanasiu, Lavinia. University of Oslo; Noruega
Fil: Bahrami, Shahram. University of Oslo; Noruega
Fil: Bailly, Henri. Université Paris Cité; Francia
Fil: Belbin, Olivia. Centro de Investigación Biomédica En Red de Enfermedades Neurodegenerativas; España. Universitat Autònoma de Barcelona; España
Fil: Bergh, Sverre. Vestfold Hospital Trust; Noruega. Innlandet Hospital Trust; Noruega
Fil: Bertram, Lars. Universität Zu Lübeck; Alemania
Fil: Biessels, Geert Jan. University of Utrecht; Países Bajos
Fil: Blennow, Kaj. University of Gothenburg; Suecia. Sahlgrenska University Hospital; Suecia
description Amyloid-beta 42 (Aβ42) and phosphorylated tau (pTau) levels in cerebrospinal fluid (CSF) reflect core features of the pathogenesis of Alzheimer’s disease (AD) more directly than clinical diagnosis. Initiated by the European Alzheimer & Dementia Biobank (EADB), the largest collaborative effort on genetics underlying CSF biomarkers was established, including 31 cohorts with a total of 13,116 individuals (discovery n = 8074; replication n = 5042 individuals). Besides the APOE locus, novel associations with two other well-established AD risk loci were observed; CR1 was shown a locus for Aβ42 and BIN1 for pTau. GMNC and C16orf95 were further identified as loci for pTau, of which the latter is novel. Clustering methods exploring the influence of all known AD risk loci on the CSF protein levels, revealed 4 biological categories suggesting multiple Aβ42 and pTau related biological pathways involved in the etiology of AD. In functional follow-up analyses, GMNC and C16orf95 both associated with lateral ventricular volume, implying an overlap in genetic etiology for tau levels and brain ventricular volume.
publishDate 2022
dc.date.none.fl_str_mv 2022-11
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/215593
The GR@ACE study group; Jansen, Iris E.; van der Lee, Sven J.; Gomez-Fonseca, Duber; de Rojas, Itziar; et al.; Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers; Springer; Acta Neuropathologica; 144; 5; 11-2022; 821-842
0001-6322
CONICET Digital
CONICET
url http://hdl.handle.net/11336/215593
identifier_str_mv The GR@ACE study group; Jansen, Iris E.; van der Lee, Sven J.; Gomez-Fonseca, Duber; de Rojas, Itziar; et al.; Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers; Springer; Acta Neuropathologica; 144; 5; 11-2022; 821-842
0001-6322
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
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info:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007/s00401-022-02454-z
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/2.5/ar/
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application/pdf
dc.publisher.none.fl_str_mv Springer
publisher.none.fl_str_mv Springer
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instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
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