伴恶性心律失常的Brugada综合征SCN1B基因突变分析1例

Fusong LIU,Fang WANG,Wenna ZHAO,Xiaobo XING,Kezhuan ZHANG,Yuzhao ZHU,Jie LIU, Ning WANG,Rong LI,Yan LIANG

Journal of Clinical Cardiology（2017）

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摘要

The SCN1B gene mutation is associated with the occurrence of Brugada syndrome.This study found that the 189th codon (T189M)of nucleotide of the SCN1B gene was the nucleotide C for T (T189M),which is a rare variation in the gene bank.It's need for further study in the family system whether the T189M of the SCN1B gene has the pathogenicity.

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