Open AccessA novel homozygous CYP19A1 gene mutation: Aromatase deficiency mimicking congenital adrenal hyperplasia in an infant without obvious maternal virilisation
Author(s) -
Fatma Dursun,
Serdar Ceylaner
Publication year - 2018
Publication title -
journal of clinical research in pediatric endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.566
H-Index - 35
eISSN - 1308-5735
pISSN - 1308-5727
DOI - 10.4274/jcrpe.0140
Subject(s) - medicine , congenital adrenal hyperplasia , aromatase , hyperplasia , mutation , endocrinology , gene , genetics , cancer , biology , breast cancer
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