Camats, NuriaUstyol, AlaAtabek, Mehmet EmreDick, BernhardFlueck, Christa E.2024-02-232024-02-2320152050-0904https://doi.org/10.1002/ccr3.343https://hdl.handle.net/20.500.12452/10545[Abstract Not Availabe]eninfo:eu-repo/semantics/openAccess17 Alpha-Hydroxylase/17,20-Lyase DeficiencyHypertensionPubertal DevelopmentSexual DevelopmentSteroidogenesisA novel CYP17A1 deletion causes a functional knockout of the steroid enzyme 17-hydroxylase and 17,20-lyase in a Turkish family and illustrates the precise role of the CYP17A1 geneArticle31079379726509008WOS:00036433000000710.1002/ccr3.343