Open AccessCytochrome P450 family 17 subfamily A member 1 mutation causes severe pseudohermaphroditism: A case report
Author(s) -
Yubin Gong,
Fang Qin,
Wenjia Li,
Le-Yu Li,
Ping He,
Xinjian Zhou
Publication year - 2022
Publication title -
world journal of clinical cases
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.368
H-Index - 10
ISSN - 2307-8960
DOI - 10.12998/wjcc.v10.i11.3553
Subject(s) - medicine , cyp17a1 , hypokalemia , congenital adrenal hyperplasia , pediatrics , male pseudohermaphroditism , blood test , endocrinology , pathology , genetics , gene , biology