Characterization of frequent deletions causing steroid 21-hydroxylase deficiency

Proceedings of the National Academy of Sciences of the United States of America

Volumn 85, Issue 12, 1988, Pages 4436-4440

  White, P C ^a   Vitek, A ^a   Dupont, B ^a   New, M I ^a  

^a WEILL CORNELL MEDICAL COLLEGE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P450;

CONGENITAL ADRENAL HYPERPLASIA; GENE CONVERSION; HLA SYSTEM; HUMAN; STEROID 21 MONOOXYGENASE DEFICIENCY;

EID: 0023749845     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.85.12.4436     Document Type: Article

References (0)