17 alpha-hydroxylase deficiency causes
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: , Mehrian Jafarizade, M.D [2]
Overview
Mutations in the CYP17A1 gene cause 17 alpha-hydroxylase deficiency. This gene is located on chromosome 10.
Causes
Mutations in the CYP17A1 gene cause 17 alpha-hydroxylase deficiency. This gene is located on chromosome 10.[1]
Reference
- ↑ Biglieri EG, Herron MA, Brust N (1966). “17-hydroxylation deficiency in man”. J. Clin. Invest. 45 (12): 1946–54. doi:10.1172/JCI105499. PMC 292880. PMID 4288776.
© 2026 MyEClinic – IFTM Institut für Telematik in der Medizin GmbH