Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine

Journal of Clinical Endocrinology and Metabolism

Volumn 85, Issue 8, 2000, Pages 2786-2792

  Pannain, Silvana ^a   Feldman, Michael ^a   Eiholzer, Urs ^b   Weiss, Roy E ^a   Scherberg, Neal H ^a   Refetoff, Samuel ^a  

^a UNIVERSITY OF CHICAGO   (United States)

^b Foundation Growth Puberty Adolescence Zurich   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ALBUMIN; MUTANT PROTEIN; PROTEIN R218P; THYROXINE; UNCLASSIFIED DRUG;

ARTICLE; CAUCASIAN; CLINICAL ARTICLE; EUTHYROIDISM; FEMALE; GENE MUTATION; HUMAN; HYPERTHYROXINEMIA; MALE; PRIORITY JOURNAL; PROTEIN BINDING; THYROXINE BLOOD LEVEL;

AMINO ACID SUBSTITUTION; CHILD, PRESCHOOL; DNA; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENOTYPE; HUMANS; HYPERTHYROXINEMIA; MALE; PEDIGREE; POINT MUTATION; SERUM ALBUMIN; SWITZERLAND; THYROXINE; TRIIODOTHYRONINE;

EID: 0034455622     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.85.8.2786     Document Type: Article

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