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Genetic variations in the 3′-untranslated region ofSLC18A2are associated with serum FSH concentration in polycystic ovary syndrome patients and regulate gene expressionin vitro
Author(s) -
Qiaoli Li,
Zheng Yan,
Yanping Kuang,
Xinyao Zhou,
Jin Li,
Lin He,
Xiaoxi Sun,
Tao Tao,
Lei Wang
Publication year - 2016
Publication title -
human reproduction
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.446
H-Index - 226
eISSN - 1460-2350
pISSN - 0268-1161
DOI - 10.1093/humrep/dew162
Subject(s) - polycystic ovary , hyperandrogenism , endocrinology , medicine , biology , single nucleotide polymorphism , insulin resistance , insulin , genetics , genotype , gene
Are genetic variations at the human solute carrier family 18 member A2 (SLC18A2) locus associated with the etiology of polycystic ovary syndrome (PCOS) and/or with follicle stimulating hormone (FSH) levels and insulin secretion in PCOS?

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