Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations-Reference-Cited by-同舟云学术

Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations

Published:2014-10-24 Issue:6 Volume:109 Page:
ISSN:0300-8428
Container-title:Basic Research in Cardiology
language:en
Short-container-title:Basic Res Cardiol

Author:

Béziau Delphine M.,Barc Julien,O’Hara Thomas,Le Gloan Laurianne,Amarouch Mohamed Yassine,Solnon Aude,Pavin Dominique,Lecointe Simon,Bouillet Patricia,Gourraud Jean-Baptiste,Guicheney Pascale,Denjoy Isabelle,Redon Richard,Mabo Philippe,le Marec Hervé,Loussouarn Gildas,Kyndt Florence,Schott Jean-Jacques,Probst Vincent,Baró Isabelle

Publisher

Springer Science and Business Media LLC

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

Link

http://link.springer.com/content/pdf/10.1007/s00395-014-0446-5.pdf

Reference34 articles.

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4. Benson DW, Wang DW, Dyment M, Knilans TK, Fish FA, Strieper MJ, Rhodes TH, George AL Jr (2003) Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A). J Clin Invest 112:1019–1028. doi: 10.1172/JCI18062

5. Berne P, Brugada J (2012) Brugada syndrome 2012. Circ J 76:1563–1571. doi: 10.1253/circj.CJ-12-0717

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