Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6)-Reference-Cited by-同舟云学术

Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6)

Published:2011-03-07 Issue:9 Volume:32 Page:1077-1088
ISSN:0195-668X
Container-title:European Heart Journal
language:en
Short-container-title:European Heart Journal

Author:

Templin C.,Ghadri J.-R.,Rougier J.-S.,Baumer A.,Kaplan V.,Albesa M.,Sticht H.,Rauch A.,Puleo C.,Hu D.,Barajas-Martinez H.,Antzelevitch C.,Luscher T. F.,Abriel H.,Duru F.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

Link

http://academic.oup.com/eurheartj/article-pdf/32/9/1077/1561512/ehr076.pdf

Reference28 articles.

1. Short QT Syndrome

2. Idiopathic Short QT Interval:A New Clinical Syndrome?

3. Congenital Short QT Syndrome and Implantable Cardioverter Defibrillator Treatment:. Inherent Risk for Inappropriate Shock Delivery

4. Short QT Interval and Short QT Syndromes

5. A Novel Form of Short QT Syndrome (SQT3) Is Caused by a Mutation in the KCNJ2 Gene

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