Presentation, Diagnosis, and Follow-Up Characteristics of 17α-Hydroxylase Deficiency Cases with Exon 1-6 Deletion (Founder Mutation) in the CYP17A1Gene: 20-Year Single-Center Experience.

Dundar, İSMAİL; Akinci, Aysehan; Camtosun, EMİNE; Ciftci, Nurdan; Kayas, Leman

doi:10.1159/000529158

Presentation, Diagnosis, and Follow-Up Characteristics of 17α-Hydroxylase Deficiency Cases with Exon 1-6 Deletion (Founder Mutation) in the CYP17A1Gene: 20-Year Single-Center Experience.

Dundar İ., Akinci A., Camtosun E., Ciftci N., Kayas L.

Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation, vol.17, no.1, pp.43-50, 2023 (SCI-Expanded)

Publication Type: Article / Article
Volume: 17 Issue: 1
Publication Date: 2023
Doi Number: 10.1159/000529158
Journal Name: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation
Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, BIOSIS, CAB Abstracts, MEDLINE, Veterinary Science Database
Page Numbers: pp.43-50
Inonu University Affiliated: Yes