Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A.
Yao-Bin ZhuJian-Hui ZhangYuan-Yuan JiYa-Nan HuHan-Lu WangDan-Dan RuanXiao-Rong MengXin-Fu LinJie-Wei LuoWei ChenPublished in: Cardiology research and practice (2022)
The newly discovered mutation site c.4313dup(p.Trp1439ValfsTer32) in exon 25 of SCN5A may be the molecular genetic basis of the family with Brugada syndrome.
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