Developmentally regulated SCN5A splice variant potentiates dysfunction of a novel mutation associated with severe fetal arrhythmia-Reference-Cited by-同舟云学术

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Developmentally regulated SCN5A splice variant potentiates dysfunction of a novel mutation associated with severe fetal arrhythmia

Published:2012-04 Issue:4 Volume:9 Page:590-597
ISSN:1547-5271
Container-title:Heart Rhythm
language:en
Short-container-title:Heart Rhythm

Author:

Murphy Lisa L.,Moon-Grady Anita J.,Cuneo Bettina F.,Wakai Ronald T.,Yu Suhong,Kunic Jennifer D.,Benson D. Woodrow,George Alfred L.

Publisher

Elsevier BV

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference34 articles.

1. Long QT and short QT syndrome;Schwartz,2009

2. De novo mutation in the SCN5A gene associated with early onset of sudden infant death;Wedekind;Circulation,2001

3. A molecular link between the sudden infant death syndrome and the long-QT syndrome;Schwartz;N Engl J Med,2000

4. Long QT syndrome and life threatening arrhythmia in a newborn: molecular diagnosis and treatment response;Schulze-Bahr;Heart,2004

5. Malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional cardiac sodium channel;Wang;Circ Arrhythm Electrophysiol,2008

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