Inherited arrhythmia syndromes: exome sequencing opens a new door to diagnosis

J Am Coll Cardiol. 2014 Jan 28;63(3):267-8. doi: 10.1016/j.jacc.2013.07.089. Epub 2013 Sep 25.

Authors

Sumeet S Chugh¹, Adriana Huertas-Vazquez²

Affiliations

¹ The Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California. Electronic address: sumeet.chugh@cshs.org.
² The Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California.

PMID: 24076289
DOI: 10.1016/j.jacc.2013.07.089

No abstract available

Publication types

Editorial
Comment

MeSH terms

Calmodulin / genetics*
DNA / genetics*
Female
Genetic Predisposition to Disease*
Humans
Male
Monomeric Clathrin Assembly Proteins / genetics*
Mutation*
Ventricular Fibrillation / genetics*

Substances

Calmodulin
Monomeric Clathrin Assembly Proteins
PICALM protein, human
DNA