A 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 gene
| dc.contributor.author | Camats, Nuria | |
| dc.contributor.author | Ustyol, Ala | |
| dc.contributor.author | Atabek, Mehmet Emre | |
| dc.contributor.author | Dick, Bernhard | |
| dc.contributor.author | Flueck, Christa E. | |
| dc.date.accessioned | 2024-02-23T12:05:57Z | |
| dc.date.available | 2024-02-23T12:05:57Z | |
| dc.date.issued | 2015 | |
| dc.department | NEÜ | en_US |
| dc.description.abstract | [Abstract Not Availabe] | en_US |
| dc.description.sponsorship | Swiss National Science Foundation [320030-146127]; Foundation Bangerter-Rhyner, Basel, Switzerland; Swiss National Science Foundation (SNF) [320030_146127] Funding Source: Swiss National Science Foundation (SNF) | en_US |
| dc.description.sponsorship | This work was supported by grants from the Swiss National Science Foundation (320030-146127) to CEF and the Foundation Bangerter-Rhyner, Basel, Switzerland to NC. | en_US |
| dc.identifier.doi | 10.1002/ccr3.343 | |
| dc.identifier.endpage | 797 | en_US |
| dc.identifier.issn | 2050-0904 | |
| dc.identifier.issue | 10 | en_US |
| dc.identifier.pmid | 26509008 | en_US |
| dc.identifier.startpage | 793 | en_US |
| dc.identifier.uri | https://doi.org/10.1002/ccr3.343 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12452/10545 | |
| dc.identifier.volume | 3 | en_US |
| dc.identifier.wos | WOS:000364330000007 | en_US |
| dc.indekslendigikaynak | Web of Science | en_US |
| dc.indekslendigikaynak | PubMed | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Wiley | en_US |
| dc.relation.ispartof | Clinical Case Reports | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | 17 Alpha-Hydroxylase/17,20-Lyase Deficiency | en_US |
| dc.subject | Hypertension | en_US |
| dc.subject | Pubertal Development | en_US |
| dc.subject | Sexual Development | en_US |
| dc.subject | Steroidogenesis | en_US |
| dc.title | A 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 gene | en_US |
| dc.type | Article | en_US |












