A Missense Mutation in the Sodium Channel β2 Subunit RevealsSCN2Bas a New Candidate Gene for Brugada Syndrome-Reference-Cited by-同舟云学术

A Missense Mutation in the Sodium Channel β2 Subunit RevealsSCN2Bas a New Candidate Gene for Brugada Syndrome

Published:2013-04-29 Issue:7 Volume:34 Page:961-966
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Riuró Helena¹²,Beltran-Alvarez Pedro¹²,Tarradas Anna¹²,Selga Elisabet¹²,Campuzano Oscar¹²,Vergés Marcel¹²,Pagans Sara¹²,Iglesias Anna¹²,Brugada Josep³,Brugada Pedro⁴,Vázquez Francisco M.⁵,Pérez Guillermo J.¹²,Scornik Fabiana S.¹²,Brugada Ramon¹²

Affiliation:

1. Cardiovascular Genetics Center; Institut d'Investigació Biomèdica de Girona (IDIBGI); Girona Spain

2. Department of Medical Science, Medical School; Universitat de Girona (UdG); Girona Spain

3. Hospital Clínic de Barcelona; Universitat de Barcelona; Barcelona Spain

4. Heart Rhythm Management Centre; UZB; Brussels Belgium

5. Servicio de Cardiología; Hospital Virgen del Rocio; Sevilla Spain

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference33 articles.

1. Cardiac sodium channel Na(v)1.5 and interacting proteins: physiology and pathophysiology;Abriel;J Mol Cell Cardiol,2010