Congenital isolated central hypothyroidism caused by a "hot spot" mutation in the thyrotropin-βgene

Thyroid

Volumn 12, Issue 12, 2002, Pages 1141-1146

  McDermott, Michael T ^a   Haugen, Bryan R ^a   Black, Jennifer N ^a   Wood, William M ^a   Gordon, David F ^a   Ridgway, E Chester ^a  

^a UNIVERSITY OF COLORADO SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; LEVOTHYROXINE; THYROTROPIN;

ADULT; ARTICLE; CASE REPORT; CODON; CONGENITAL HYPOTHYROIDISM; EUROPE; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENE MUTATION; HORMONE DEFICIENCY; HUMAN; MALE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SOUTH AMERICA; THYROTROPIN BLOOD LEVEL; UNITED STATES;

EID: 0036961873     PISSN: 10507256     EISSN: None     Source Type: Journal    
DOI: 10.1089/105072502321085252     Document Type: Article

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