The Structure of the Coding and 5′-Flanking Region of the Type 1 Iodothyronine Deiodinase (dio1) Gene Is Normal in a Patient with Suspected Congenital dio1 Deficiency

Journal of Clinical Endocrinology and Metabolism

Volumn 81, Issue 6, 1996, Pages 2121-2124

  Toyoda, Nagaoki ^a   Kleinhaus, Noemi ^b   Larsen, P Reed ^a  

^a HARVARD MEDICAL SCHOOL   (United States)

^b Linn Clinic   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

THYROXINE DEIODINASE;

ADULT; ARTICLE; CASE REPORT; DEIODINATION; DNA FLANKING REGION; ENZYME ACTIVE SITE; ENZYME ACTIVITY; ENZYME DEFICIENCY; EXON; FEMALE; GENE REARRANGEMENT; GENE SEQUENCE; GENE STRUCTURE; HORMONE RESISTANCE; HUMAN; HYPERTHYROXINEMIA; INTRON; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; BASE SEQUENCE; CLONING, MOLECULAR; DNA; GENE EXPRESSION; GENES; HUMANS; IODIDE PEROXIDASE; MOLECULAR SEQUENCE DATA; PROMOTER REGIONS (GENETICS); REFERENCE VALUES;

EID: 0029888627     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jcem.81.6.8964838     Document Type: Article

References (20)

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