Targovnik, H. M., Edouard, T., Varela, V., Tauber, M., Citterio, C. E., González Sarmiento, R., & Rivolta, C. M. (2012). Two novel mutations in the thyroglobulin gene as cause of congenital hypothyroidism: Identification a cryptic donor splice site in the exon 19. Web
Citación estilo ChicagoTargovnik, Hector Manuel, Thomas Edouard, Viviana Varela, Maithé Tauber, Cintia Eliana Citterio, Rogelio González Sarmiento, and Carina Marcela Rivolta. Two Novel Mutations in the Thyroglobulin Gene As Cause of Congenital Hypothyroidism: Identification a Cryptic Donor Splice Site in the Exon 19. 2012.
Cita MLATargovnik, Hector Manuel, et al. Two Novel Mutations in the Thyroglobulin Gene As Cause of Congenital Hypothyroidism: Identification a Cryptic Donor Splice Site in the Exon 19. 2012.