The global distribution of the p.R1193Q polymorphism in the SCN5A gene

Author:

Matsusue Aya,Yuasa Isao,Umetsu Kazuo,Nakayashiki Nori,Dewa Koji,Nishimukai Hiroaki,Kashiwagi Masayuki,Hara Kenji,Waters Brian,Takayama Mio,Ikematsu Natsuki,Kubo Shin-ichi

Funder

Grants-in-Aid for Scientific Research (C)

Grant-in-Aid for Young Scientists (B)

Publisher

Elsevier BV

Subject

Issues, ethics and legal aspects,Pathology and Forensic Medicine

Reference27 articles.

1. Effects of mutations and genetic overlap in inherited long-QT and Brugada arrhythmia syndromes;Kotta;Hellenic J. Cardiol.,2012

2. The genetic component of Brugada syndrome;Nielsen;Front. Physiol.,2013

3. Sodium channel mutations and arrhythmias;Ruan;Nat. Rev. Cardiol.,2009

4. The common SCN5A mutation R1193Q causes LQTS-type electrophysiological alterations of the cardiac sodium channel;Wang;J. Med. Genet.,2004

5. Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome;Vatta;Hum. Mol. Genet.,2002

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