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Letter by Jin-shan and Xue-bin Regarding Article, "Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter Registry".

作者信息

Jin-Shan He, Xue-Bin Li

机构信息

Department of Cardiology, Beijing Key Laboratory of Early Prediction and Intervention of Acute Myocardial Infarction, Peking University People's Hospital, Beijing, China.

出版信息

Circulation. 2017 Dec 5;136(23):2287-2288. doi: 10.1161/CIRCULATIONAHA.117.030553.

DOI:10.1161/CIRCULATIONAHA.117.030553
PMID:29203569
Abstract
摘要

相似文献

1
Letter by Jin-shan and Xue-bin Regarding Article, "Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter Registry".金山和薛斌就文章《Brugada综合征先证者临床及心电图特征的SCN5A突变基因型-表型相关性:一项日本多中心注册研究》所写的信函
Circulation. 2017 Dec 5;136(23):2287-2288. doi: 10.1161/CIRCULATIONAHA.117.030553.
2
Response by Yamagata et al to Letter Regarding Article, "Genotype-Phenotype Correlation of Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter Registry".山形等人对关于文章《Brugada综合征先证者突变的基因型-表型相关性与临床及心电图特征:一项日本多中心注册研究》的信件的回复
Circulation. 2017 Dec 5;136(23):2289-2290. doi: 10.1161/CIRCULATIONAHA.117.030845.
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Genotype-Phenotype Correlation of Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter Registry.Brugada 综合征先证者基因突变的临床和心电图特征的基因型-表型相关性:日本多中心注册研究。
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Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation.1型强直性肌营养不良模拟并加重由Nav1.5钠通道功能丧失突变诱导的Brugada表型。
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Copy number variations of SCN5A in Brugada syndrome.Brugada 综合征中 SCN5A 的拷贝数变异。
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Identification of a SCN5A founder mutation causing sudden death, Brugada syndrome, and conduction blocks in Southern Italy.在意大利南部发现 SCN5A 致病变异导致心源性猝死、Brugada 综合征和传导阻滞。
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