Molecular modeling and clinical characterization of a CYP17A1 variant (p.Asp298Asn) causing 17α-hydroxylase/17,20-lyase deficiency in two siblings
- DOI
- 10.1297/cpe.2026-0009
- Published
- 2026
- Container
- Clinical Pediatric Endocrinology
- Publisher
- Japanese Society for Pediatric Endocrinology
- Open access
- unknown
Credibility signals
uncertain Score 64/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
Show all credibility signals
- supportingDOI registered: A matching record was returned by Crossref.
- supportingDOI resolves: A matching record was returned by Crossref.
- not scoredDirectory of Open Access Journals: No matching DOAJ record was present in this response. No allow-list match; this is not evidence of low credibility.
- not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made.
- not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made.
- not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made.
- not scoredROR affiliation: Not checked or no result supplied; no credibility inference made.
- not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch expression of concern: No expression of concern notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredOpen access status: Not checked or no result supplied; no credibility inference made.
- not scoredPublication license: Not checked or no result supplied; no credibility inference made.
- not scoredPublication version: A publication version was supplied but is not scored.
- supportingMetadata completeness: All 6 scored descriptive metadata groups are present.
Cite this work
BibTeX
@article{allodium:10.1297/cpe.2026-0009,
title = {Molecular modeling and clinical characterization of a CYP17A1 variant (p.Asp298Asn) causing 17α-hydroxylase/17,20-lyase deficiency in two siblings},
author = {Ertugrul Sancak and Muammer Büyükinan and Ahmet Fatih Yılmaz and Berna Karslı and Ebru Marzioğlu Özdemir and Bayram Toraman and Fuat Buğrul and Fatma Özgüç Çömlek},
year = {2026},
journal = {Clinical Pediatric Endocrinology},
doi = {10.1297/cpe.2026-0009},
url = {https://doi.org/10.1297/cpe.2026-0009}
}RIS
TY - JOUR TI - Molecular modeling and clinical characterization of a CYP17A1 variant (p.Asp298Asn) causing 17α-hydroxylase/17,20-lyase deficiency in two siblings AU - Ertugrul Sancak AU - Muammer Büyükinan AU - Ahmet Fatih Yılmaz AU - Berna Karslı AU - Ebru Marzioğlu Özdemir AU - Bayram Toraman AU - Fuat Buğrul AU - Fatma Özgüç Çömlek PY - 2026 JO - Clinical Pediatric Endocrinology DO - 10.1297/cpe.2026-0009 UR - https://doi.org/10.1297/cpe.2026-0009 ER -
APA
Sancak, E., Büyükinan, M., Yılmaz, A. F., Karslı, B., Özdemir, E. M., Toraman, B., Buğrul, F., & Çömlek, F. Ö. (2026). Molecular modeling and clinical characterization of a CYP17A1 variant (p.Asp298Asn) causing 17α-hydroxylase/17,20-lyase deficiency in two siblings. Clinical Pediatric Endocrinology. https://doi.org/10.1297/cpe.2026-0009
Source records
- crossref · retrieved 2026-09-25T08:13:10.686Z