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, cilt.17, sa.1, ss.43-50, 2023 (SCI-Expanded, Scopus)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 17 Sayı: 1
Basım Tarihi: 2023
Doi Numarası: 10.1159/000529158
Dergi Adı: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, BIOSIS, CAB Abstracts, MEDLINE, Veterinary Science Database
Sayfa Sayıları: ss.43-50
İnönü Üniversitesi Adresli: Evet