ACTN2:

Bo Lan1,2,3,4, Zhiyu Liu1,2,3,4, Jing Bai1,2,3,4

  • 1Department of Cardiology, The First Affiliated Hospital of Zhengzhou University, No. 1, Jianshe East Road, Erqi District, Zhengzhou, Henan 450052, China.

PubMed
概括

家庭限制性心肌病 (RCM) 是罕见的. 在一个患有昏迷和心脏骤停的年轻男性身上发现了一种新的ACTN2基因突变,证实了它在他的家人突然心脏死亡中的作用.

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