Whole-exome sequencing reveals genetic variants in ERC1 and KCNG4 associated with complete hydatidiform mole in Chinese Han women

Complete hydatidiform mole (CHM) is a rare pregnancy-related disease with invasive potential. The genetics underlying the sporadic form of CHM have not been addressed previously, but maternal genetic variants may be involved in biparental CHM. We performed whole-exome sequencing of 51 patients with...

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Detalhes bibliográficos
Publicado no:Oncotarget
Main Authors: Yu, Yan, Lu, Bingjian, Lu, Weiguo, Li, Shuang, Li, Xiuqin, Wang, Xinyu, Wan, Xiaoyun, Chen, Yaxia, Feng, Suwen, Jia, Yao, Yang, Ru, Tang, Fangxu, Li, Xiong, Zhang, Shulan, Wang, Xinyan, Wei, Heng, Peng, Zhilan, Lu, Lin, Zhong, Huizhen, Zhao, Linjun, Huang, Zhangqian, Lin, Lin, Shen, Weihong, Lu, Yan, Cao, Zhu, Zou, Jian, Ma, Yuejiang, Chen, Xiaojing, Tian, Qifang, Lu, Shiming, Liu, Pengyuan, Ma, Ding, Xie, Xing, Cheng, Xiaodong
Formato: Artigo
Idioma:Inglês
Publicado em: Impact Journals LLC 2017
Assuntos:
Research Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5650418/
https://ncbi.nlm.nih.gov/pubmed/29088863
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.20769
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