Functional analysis of four CYP21 mutations from Spanish patients with congenital adrenal hyperplasia

Biochemical and Biophysical Research Communications

Volumn 262, Issue 3, 1999, Pages 635-637

  Nunez, B Scott ^a   Lobato, M Natividad ^b   White, Perrin C ^a   Meseguer, Anna ^b  

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

^b HOSPITAL UNIVERSITARI VALL D HEBRON   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROXYPROGESTERONE; PROGESTERONE; STEROID 21 MONOOXYGENASE;

ARTICLE; CLINICAL ARTICLE; CONGENITAL ADRENAL HYPERPLASIA; ENZYME ACTIVITY; ENZYME SUBSTRATE; GENE CONVERSION; GENE DELETION; GENE MUTATION; GENETIC RECOMBINATION; HUMAN; NONSENSE MUTATION; POINT MUTATION; PRIORITY JOURNAL; PSEUDOGENE;

EID: 0033533579     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.1999.1271     Document Type: Article

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