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Volumn 85, Issue 5, 1988, Pages 1600-1604
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Mutation in the CYP21B gene (Ile-172→Asn) causes steroid 21-hydroxylase deficiency
a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
STEROID 21 MONOOXYGENASE;
CONGENITAL ADRENAL HYPERPLASIA;
HUMAN;
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EID: 0007383587
PISSN: 00278424
EISSN: None
Source Type: Journal
DOI: 10.1073/pnas.85.5.1600 Document Type: Article |
Times cited : (215)
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References (0)
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