Mutations in DMC1 are not responsible for premature ovarian failure in Chinese women

被引：8
|
作者：
Wang, Huidan [1 ]
Sun, Mei [1 ]
Qin, Yingying [1 ]
Xia, Tingting [2 ]
Ma, Jinlong [1 ]
Chen, Zi-Jiang [1 ]
机构：
[1] Shandong Univ, Prov Hosp,Key Lab Reprod Endocrinol, Minist Educ,Ctr Reprod Med,Shandong Prov Key Lab, Natl Res Ctr Assisted Reprod Technol & Reprod Gen, Jinan 250021, Peoples R China
[2] Sun Yat Sen Univ Med Sci, Affiliated Hosp 1, Guangzhou 510080, Guangdong, Peoples R China
来源：
REPRODUCTIVE BIOMEDICINE ONLINE | 2013年 / 26卷 / 02期
基金：
中国国家自然科学基金;
关键词：
DMC1; mutation; premature ovarian failure; single-nucleotide polymorphism; FOLLICLE-STIMULATING-HORMONE; CHROMOSOME SYNAPSIS; BETA-SUBUNIT; RECEPTOR; GENE; INSUFFICIENCY; EXPRESSION; RESISTANCE; MEIOSIS; HOMOLOG;
D O I：
10.1016/j.rbmo.2012.10.016
中图分类号：
R71 [妇产科学];
学科分类号：
100211 ;
摘要：
The coding region of the disrupted meiotic cDNA gene (DMC1) was examined in 192 Chinese women with premature ovarian failure. Two known single-nucleotide polymorphisms, c.8632C>T in intron 4 and c.32377G>C in intron 10, were identified. The results suggest that mutations in the coding sequence of DMC1 are not associated with premature ovarian failure in Chinese women. RBMOnline (C) 2012, Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码：175 / 178
页数：4
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