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A newly identified missense mutation in CLCA2 is associated with autosomal dominant cardiac conduction block

A newly identified missense mutation in CLCA2 is associated with autosomal dominant cardiac conduction block

Mao, Zhuo; Wang, Yi; Peng, Hao; He, Fang; Zhu, Li; Huang, He; Huang, Xianghong; Lu, Xiaowei; Tan, Xiaojun
  • 期刊名称Gene
  • 作者Mao, Zhuo; Wang, Yi; Peng, Hao; He, Fang; Zhu, Li; Huang, He; Huang, Xianghong; Lu, Xiaowei; Tan, Xiaojun
  • 印刷ISSN0378-1119
  • 文件大小716.08KB
  • 发表时间2019-7
  • DOI10.1016/j.gene.2019.143990
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