A mutation (pro-30 to leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele

Molecular Endocrinology

Volumn 5, Issue 5, 1991, Pages 685-692

  Tusie Luna, Maria Teresa ^a,b   Speiser, Phyllis W ^a,b   Dumic, Miro ^a,b   New, Maria I ^a,b   White, Perrin C ^a,b  

^a WEILL CORNELL MEDICAL COLLEGE   (United States)

^b Croatia   (Croatia)

Author keywords

[No Author keywords available]

Indexed keywords

STEROID 21 MONOOXYGENASE;

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; HUMAN; MALE; MOLECULAR BIOLOGY; MUTATION; PRIORITY JOURNAL; STEROIDOGENESIS;

ADRENAL HYPERPLASIA, CONGENITAL; ALLELES; ANIMAL; BASE SEQUENCE; FEMALE; HUMAN; LEUCINE; MALE; MOLECULAR SEQUENCE DATA; MUTATION; NUCLEIC ACID HYBRIDIZATION; PEDIGREE; PROLINE; RABBITS; RECOMBINANT PROTEINS; STEROID 21-HYDROXYLASE; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; VACCINIA VIRUS;

VACCINIA; VACCINIA VIRUS;

EID: 0025773734     PISSN: 08888809     EISSN: 19449917     Source Type: Journal    
DOI: 10.1210/mend-5-5-685     Document Type: Article

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