A new compound heterozygous for c.886C>T/c.2206C>T [p.R277X/p.Q717X] mutations in the thyroglobulin gene as a cause of foetal goitrous hypothyroidism

✍ Scribed by Cintia E. Citterio; Regis Coutant; Stephanie Rouleau; José M. Miralles García; Rogelio Gonzalez-Sarmiento; Carina M. Rivolta; Héctor M. Targovnik

• Book ID: 108704797
• Publisher: John Wiley and Sons
• Year: 2011
• Tongue: English
• Weight: 122 KB
• Volume: 74
• Category: Article
• ISSN: 0300-0664
• DOI: 10.1111/j.1365-2265.2010.03932.x