Novel mutations in domain I of SCN5A cause Brugada syndrome-Reference-Cited by-同舟云学术

Novel mutations in domain I of SCN5A cause Brugada syndrome

Published:2002-04 Issue:4 Volume:75 Page:317-324
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Vatta Matteo,Dumaine Robert,Antzelevitch Charles,Brugada Ramon,Li Hua,Bowles Neil E.,Nademanee Koonlawee,Brugada Josep,Brugada Pedro,Towbin Jeffrey A.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference29 articles.

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4. Ion channels and ventricular arrhythmias: Cellular and ionic mechanisms underlying the Brugada syndrome;Antzelevitch;Curr. Opin. Cardiol.,1999

5. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation;Chen;Nature,1998

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