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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650418/
https://www.ncbi.nlm.nih.gov/pubmed/29088863
http://dx.doi.org/10.18632/oncotarget.20769

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