Congenital hypothyroidism in a child with unsuspected familial dysalbuminemic hyperthyroxinemia caused by a mutation (R218H) in the human albumin gene

✍ Scribed by Joachim Pohlenz; Peter M. Sadow; Thomas Koffler; Winfried Schönberger; Roy E. Weiss; Samuel Refetoff

• Book ID: 117847941
• Publisher: Elsevier Science
• Year: 2001
• Tongue: English
• Weight: 156 KB
• Volume: 139
• Category: Article
• ISSN: 1097-6833
• DOI: 10.1067/mpd.2001.119594