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A novel homozygous frame‐shift variant in the LHCGR gene is associated with primary ovarian insufficiency in a Pakistani family
Author(s) -
Zielen A.C.,
Khan M.J.,
Pollock N.,
Jiang H.,
Ahmed J.,
Nazli R.,
Jabeen M.,
Yatsenko A.,
Rajkovic A.
Publication year - 2018
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.13406
Subject(s) - gene , genetics , medicine , biology , endocrinology