Whole exome sequencing identifies the TNNI3K gene as a cause of familial conduction system disease and congenital junctional ectopic tachycardia-Reference-Cited by-同舟云学术

Whole exome sequencing identifies the TNNI3K gene as a cause of familial conduction system disease and congenital junctional ectopic tachycardia

Published:2015-04 Issue: Volume:185 Page:114-116
ISSN:0167-5273
Container-title:International Journal of Cardiology
language:en
Short-container-title:International Journal of Cardiology

Author:

Xi Yanwei,Honeywell Christina,Zhang Dapeng,Schwartzentruber Jeremy,Beaulieu Chandree L.,Tetreault Martine,Hartley Taila,Marton Jennifer,Vidal Silvia M.,Majewski Jacek,Aravind L.,Gollob Michael,Boycott Kym M.,Gow Robert M.

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

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3. Mutations in riboflavin transporter present with severe sensory loss and deafness in childhood;Srour;Muscle Nerve,2014

4. TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy;Theis;Hum. Mol. Genet.,2014

5. Evidence, hypotheses and significance of MAP kinase TNNI3K interacting with its partners;Lai;World J. Hypertens.,2012

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