Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD
Neşe AkcanZehra Oya UygunerFirdevs BaşUmut AltunogluGüven ToksoyBirsen KaramanSahin AvciZehra Yavaş AbalıŞükran PoyrazoğluAgharza AghayevVolkan KaramanRüveyde BundakSeher BaşaranFeyza DarendelılerPublished in: Journal of clinical research in pediatric endocrinology (2022)
variants were identified in our study.