Scopus WoS Açık Erişim
Q3
★ Oto
ESCI Hakemli
Molecular modeling and clinical characterization of a CYP17A1 variant (p. Asp298Asn) causing 17α-hydroxylase/17, 20-lyase deficiency in two siblings
Clinical Pediatric Endocrinology · 2026 · Cilt 1 · Sayı 1