Case Report

Aromatase Deficiency in Two Siblings with 46, XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in CYP19A1 Gene
  • Samim Ozen
  • Tahir Atik
  • Ozlem Korkmaz
  • Huseyin Onay
  • Damla Goksen
  • Ferda Ozkınay
  • Ozgur Cogulu
  • Sukran Darcan
J Clin Res Pediatr Endocrinol 0; 0: 0-0 [e-Pub] DOI: 10.4274/jcrpe.galenos.2019.2018.0198 PMID:30968679
A Novel Homozygous CYP19A1 Gene Mutation: Aromatase Deficiency Mimicking Congenital Adrenal Hyperplasia in an Infant without Obvious Maternal Virilisation
  • Fatma Dursun
  • Serdar Ceylaner
J Clin Res Pediatr Endocrinol 2019; 11: 196-201 DOI: 10.4274/jcrpe.galenos.2018.2018.0140 PMID:30074481
Aromatase Deficiency due to a Novel Mutation in CYP19A1 Gene
  • Edip Unal
  • Ruken Yıldırım
  • Funda Feryal Taş
  • Vasfiye Demir
  • Hüseyin Onay
  • Yusuf Kenan Haspolat
J Clin Res Pediatr Endocrinol 2018; 10: 377-381 DOI: 10.4274/jcrpe.0011 PMID:29553041

Original Research

A Novel Null Mutation in P450 Aromatase Gene (CYP19A1) Associated with Development of Hypoplastic Ovaries in Humans
  • Sema Akçurin
  • Doğa Türkkahraman
  • Woo-Young Kim
  • Erdem Durmaz
  • Jae-Gook Shin
  • Su-Jun Lee
J Clin Res Pediatr Endocrinol 2016; 8: 205-210 DOI: 10.4274/jcrpe.2761 PMID:27086564

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