A rare cause of delayed puberty in two cases with 46,XX and 46,XY karyotype: 17 α-hydroxylase deficiency due to a novel variant in CYP17A1 gene-Reference-Cited by-同舟云学术

A rare cause of delayed puberty in two cases with 46,XX and 46,XY karyotype: 17 α-hydroxylase deficiency due to a novel variant in CYP17A1 gene

Author:

Unal Edip¹,Yıldırım Ruken²,Taş Funda Feryal¹,Tekin Suat³,Ceylaner Serdar⁴,Haspolat Yusuf Kenan¹

Affiliation:

1. Department of Pediatric Endocrinology, Dicle University Medical Faculty, Diyarbakir, Turkey;

2. Department of Pediatric Endocrinology, Diyarbakır Children's Hospital, Diyarbakir, Turkey;

3. Department of Pediatrics, Dicle University Medical Faculty, Diyarbakir, Turkey;

4. Intergen Genetic Diagnosis Center, Department of Medical Genetics, Ankara, Turkey

Publisher

Informa UK Limited

Subject

Obstetrics and Gynaecology,Endocrinology,Endocrinology, Diabetes and Metabolism

Link

Reference13 articles.

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