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GENETIC MARKER FOR POLYCYSTIC OVARY SYNDROME (PCOS)

机译:多囊卵巢综合征(PCOS)的遗传标记

摘要

The present invention relates to a novel genetic marker for polycystic ovary syndrome (PCOS), and in particular to a method for diagnosing polycystic ovary syndrome (PCOS) or detecting a predisposition of a female subject to polycystic ovary syndrome (PCOS), comprising examining the human annexin A5 (ANXA5) promoter in a sample obtained from the female subject and to detect nucleotide exchanges therein. The present invention also relates to a nucleic acid sequence comprising a human annexin A5 (ANXA5) promoter, which promoter comprises specific nucleotide exchanges defined herein, for use in the methods disclosed herein. The present invention further relates to a kit for use in the diagnostic methods disclosed herein.
机译:本发明涉及一种用于多囊卵巢综合征(PCOS)的新型遗传标记,尤其涉及一种诊断多囊卵巢综合征(PCOS)或检测女性受试者多囊卵巢综合征(PCOS)的易感性的方法,包括检查得自女性受试者的样品中的人膜联蛋白A5(ANXA5)启动子,并检测其中的核苷酸交换。本发明还涉及包含人膜联蛋白A5(ANXA5)启动子的核酸序列,该启动子包含本文定义的特定核苷酸交换,用于本文公开的方法。本发明进一步涉及用于本文公开的诊断方法的试剂盒。

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