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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?

human reproduction

Genetic variations in the 3′-untranslated region of<i>SLC18A2</i>are associated with serum FSH concentration in polycystic ovary syndrome patients and regulate gene expression<i>in vitro</i>

Genetic variations in the 3′-untranslated region ofSLC18A2are associated with serum FSH concentration in polycystic ovary syndrome patients and regulate gene expressionin vitro