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

• 1 December 2001
• journal article
• case report
• Published by Elsevier in The Journal of Pediatrics
• Vol. 139  (6) , 887-891
• https://doi.org/10.1067/mpd.2001.119594

Abstract

Keywords

• BINDING PROTEIN
• SERUM ALBUMIN
• DNA ANALYSIS
• ISOELECTRIC FOCUSING

Funding Information

• Novo Nordisk (DK 15070)
• National Institutes of Health