Molecular genetics and pathophysiology of 17β-hydroxysteroid dehydrogenase 3 deficiency

Journal of Clinical Endocrinology and Metabolism

Volumn 81, Issue 1, 1996, Pages 130-136

  Andersson, Stefan ^a   Geissler, Wayne M ^a   Wu, Ling ^a   Davis, Daphne L ⁱ   Grumbach, Melvin M ^b   New, Maria I ^c   Schwarz, Hans P ^d   Blethen, Sandra L ^e   Mendonca, Berenice B ^f   Bloise, Walter ^f   Witchel, Selma F ^g   Cutler Jr , Gordon B ^h   Griffin, James E ^j   Wilson, Jean D ^j   Russell, David W ^i,j  

^a MERCK RESEARCH LABORATORIES   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c WEILL CORNELL MEDICAL CENTER   (United States)

^d UNIVERSITY OF MUNICH   (Germany)

^e STONY BROOK UNIVERSITY   (United States)

^f UNIVERSITY OF SÃO PAULO   (Brazil)

^g UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

^h EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT   (United States)

ⁱ Department of Molecular Genetics ^*  (United States)

^j UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

TESTOSTERONE; TESTOSTERONE 17BETA DEHYDROGENASE;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHILD; CLINICAL ARTICLE; ENZYME DEFICIENCY; FRAMESHIFT MUTATION; HUMAN; INFANT; MALE; MISSENSE MUTATION; NEWBORN; PRIORITY JOURNAL; REPORTER GENE; TESTOSTERONE BLOOD LEVEL;

17-HYDROXYSTEROID DEHYDROGENASES; ADOLESCENT; ADULT; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; FEMALE; HUMANS; ISOENZYMES; MALE; MOLECULAR SEQUENCE DATA; MUTATION; TESTOSTERONE;

EID: 0344819243     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.81.1.130     Document Type: Article

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