Carro, G. H., Martín, M., Savy, S., Peyret, V., Geysels, R. C., Montes, F. A., . . . Nicola, J. P. (2024). Functional characterization of novel compound heterozygous missense SLC5A5 gene variants causing congenital dyshormonogenic hypothyroidism. Web
Citación estilo ChicagoCarro, Gerardo Hernán, et al. Functional Characterization of Novel Compound Heterozygous Missense SLC5A5 Gene Variants Causing Congenital Dyshormonogenic Hypothyroidism. 2024.
Cita MLACarro, Gerardo Hernán, et al. Functional Characterization of Novel Compound Heterozygous Missense SLC5A5 Gene Variants Causing Congenital Dyshormonogenic Hypothyroidism. 2024.
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