Aromatase Deficiency in Two Siblings with 46, XX KaryotypeRraised as Different Genders: A Novel Mutation (p.R115X) in CYP19A1 Gene

Articles > Case Report · 2019

Authors: Samim ÖZEN, Tahir ATİK, Özlem Korkmaz, HÜSEYİN ONAY, Ruhsar Damla GÖKŞEN, Feriştah Ferda ÖZKINAY, Muhsin Özgür ÇOĞULU, Şükran DARCAN

Journal of Clinical Research in Pediatric Endocrinology, Journal Indexed in SCI Expanded, International, 2019, vol 0, pp 0-0

DOI: 10.4274/jcrpe.galenos.2019.2018.0198

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