Molecular modeling and clinical characterization of a CYP17A1 variant (p. Asp298Asn) causing 17α-hydroxylase/17, 20-lyase deficiency in two siblings
CLINICAL PEDIATRIC ENDOCRINOLOGY, vol.000, no.000, pp.1-5, 2026 (ESCI, Scopus)
- Publication Type: Article / Case Report
- Volume: 000 Issue: 000
- Publication Date: 2026
- Journal Name: CLINICAL PEDIATRIC ENDOCRINOLOGY
- Journal Indexes: Scopus, Emerging Sources Citation Index (ESCI), EMBASE
- Page Numbers: pp.1-5
- Karadeniz Technical University Affiliated: Yes