The hypothyroidism in an inbred kindred with congenital thyroid hormone and glucocorticoid deficiency is due to a mutation producing a truncated thyrotropin receptor

Thyroid

Volumn 9, Issue 9, 1999, Pages 887-894

  Tiosano, Dov ^b   Pannain, Silvana ^a   Vassart, Gilbert ^c   Parma, Jasmine ^c   Gershoni Baruch, Ruth ^b   Mandel, Hanna ^b   Lotan, Rachel ^b   Zaharan, Yunes ^b   Pery, Menuha ^b   Weiss, Roy E ^a   Refetoff, Samuel ^a   Hochberg, Ze'ev ^b  

^a UNIVERSITY OF CHICAGO   (United States)

^b RAMBAM MEDICAL CENTER   (Israel)

^c UNIVERSITÉ LIBRE DE BRUXELLES   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOTROPIN; THYROTROPIN; THYROTROPIN RECEPTOR;

ADOLESCENT; ADRENAL CORTEX INSUFFICIENCY; ARTICLE; CHILD; CLINICAL ARTICLE; CODON; CORTICOTROPIN BLOOD LEVEL; FAMILY HISTORY; FEMALE; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HUMAN; HYPOTHYROIDISM; MALE; NUCLEIC ACID BASE SUBSTITUTION; PATHOGENESIS; PEDIGREE ANALYSIS; POINT MUTATION; PRIORITY JOURNAL; THYROTROPIN BLOOD LEVEL;

EID: 0032881333     PISSN: 10507256     EISSN: None     Source Type: Journal    
DOI: 10.1089/thy.1999.9.887     Document Type: Article

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