Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome | Zendy

Kenichiro Yamagata | Zendy; Minoru Horie | Zendy; Takeshi Aiba | Zendy; Satoshi Ogawa | Zendy; Yoshifusa Aizawa | Zendy; Tohru Ohe | Zendy; Masakazu Yamagishi | Zendy; Naomasa Makita | Zendy; Harumizu Sakurada | Zendy; Toshihiro Tanaka | Zendy; Akihiko Shimizu | Zendy; Nobuhisa Hagiwara | Zendy; Ryoji Kishi | Zendy; Yukiko Nakano | Zendy; Masahiko Takagi | Zendy; Takeru Makiyama | Zendy; Seiko Ohno | Zendy; Keiichi Fukuda | Zendy; Hiroshi Watanabe | Zendy; Hiroshi Morita | Zendy; Kenshi Hayashi | Zendy; Kengo Kusano | Zendy; Shiro Kamakura | Zendy; Satoshi Yasuda | Zendy; Hisao Ogawa | Zendy; Yoshihiro Miyamoto | Zendy; Jamie D. Kapplinger | Zendy; Michael J. Ackerman | Zendy; Wataru Shimizu | Zendy

Open Access

Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome

Author(s) -

Kenichiro Yamagata,

Minoru Horie,

Takeshi Aiba,

Satoshi Ogawa,

Yoshifusa Aizawa,

Tohru Ohe,

Masakazu Yamagishi,

Naomasa Makita,

Harumizu Sakurada,

Toshihiro Tanaka,

Akihiko Shimizu,

Nobuhisa Hagiwara,

Ryoji Kishi,

Yukiko Nakano,

Masahiko Takagi,

Takeru Makiyama,

Seiko Ohno,

Keiichi Fukuda,

Hiroshi Watanabe,

Hiroshi Morita,

Kenshi Hayashi,

Kengo Kusano,

Shiro Kamakura,

Satoshi Yasuda,

Hisao Ogawa,

Yoshihiro Miyamoto,

Jamie D. Kapplinger,

Michael J. Ackerman,

Wataru Shimizu

Publication year - 2017

Publication title -

circulation

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 7.795

H-Index - 607

eISSN - 1524-4539

pISSN - 0009-7322

DOI - 10.1161/circulationaha.117.027983

Subject(s) - brugada syndrome , medicine , hazard ratio , proband , cardiology , qrs complex , sudden cardiac death , genotype , mutation , confidence interval , genetics , biology , gene

The genotype-phenotype correlation of SCN5A mutations as a predictor of cardiac events in Brugada syndrome remains controversial. We aimed to establish a registry limited to probands, with a long follow-up period, so that the genotype-phenotype correlation of SCN5A mutations in Brugada syndrome can be examined without patient selection bias.

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