A novel mutation in the albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of bangladeshi extraction

Thyroid

Volumn 24, Issue 6, 2014, Pages 945-950

  Greenberg, Solomon Maximo ^a   Ferrara, Alfonso Massimiliano ^a   Nicholas, Everton S ^b   Dumitrescu, Alexandra M ^a   Cody, Vivian ^c   Weiss, Roy E ^a   Refetoff, Samuel ^a  

^a UNIVERSITY OF CHICAGO   (United States)

^b TORONTO EAST GENERAL HOSPITAL   (Canada)

^c HAUPTMAN WOODWARD MEDICAL RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALBUMIN; LIOTHYRONINE; MUTANT PROTEIN; THYROID HORMONE; THYROTROPIN; THYROXINE; 3,3',5' TRIIODOTHYRONINE; SERUM ALBUMIN;

ADULT; ALBUMIN GENE; AMINO ACID SUBSTITUTION; ARTICLE; BANGLADESH; BINDING AFFINITY; CASE REPORT; CODON; DISEASE SEVERITY; EXON; FAMILIAL DYSALBUMINEMIC HYPERTHYROXINEMIA; FEMALE; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; HUMAN; LIOTHYRONINE BLOOD LEVEL; MALE; PRIORITY JOURNAL; THYROID FUNCTION TEST; THYROXINE BLOOD LEVEL; ASIAN CONTINENTAL ANCESTRY GROUP; BLOOD; CANADA; ETHNOLOGY; GENETICS; MUTATION; PEDIGREE; YOUNG ADULT;

ASIAN CONTINENTAL ANCESTRY GROUP; BANGLADESH; CANADA; FEMALE; HUMANS; HYPERTHYROXINEMIA, FAMILIAL DYSALBUMINEMIC; MUTATION; PEDIGREE; SERUM ALBUMIN; THYROXINE; TRIIODOTHYRONINE; TRIIODOTHYRONINE, REVERSE; YOUNG ADULT;

EID: 84902148314     PISSN: 10507256     EISSN: 15579077     Source Type: Journal    
DOI: 10.1089/thy.2013.0540     Document Type: Article

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