Phenotypical Manifestations of Mutations in the Genes Encoding Subunits of the Cardiac Sodium Channel-Reference-Cited by-同舟云学术

Phenotypical Manifestations of Mutations in the Genes Encoding Subunits of the Cardiac Sodium Channel

Published:2011-04 Issue:7 Volume:108 Page:884-897
ISSN:0009-7330
Container-title:Circulation Research
language:en
Short-container-title:Circ Res

Author:

Wilde Arthur A.M.¹,Brugada Ramon¹

Affiliation:

1. From the Heart Research Centre (A.A.M.W.), Department of Clinical and Experimental Cardiology, Academic Medical Center, University Medical Center, University of Amsterdam, The Netherlands; and the Institut d'Investigació Biomèdica Girona-IdIBGi (R.B.), Universitat de Girona, Giona Spain.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

Reference112 articles.

1. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

2. Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

3. Cardiac conduction defects associate with mutations in SCN5A

4. Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

5. Cardiac sodium channel mutation in atrial fibrillation

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