Exome sequencing identifies a mutation in the ACTN2 gene in a family with idiopathic ventricular fibrillation, left ventricular noncompaction, and sudden death
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Title
Exome sequencing identifies a mutation in the ACTN2 gene in a family with idiopathic ventricular fibrillation, left ventricular noncompaction, and sudden death
Authors
Keywords
Phenotype heterogeneity, Arrhythmia, Cardiomyopathy, Exome sequencing
Journal
BMC Medical Genetics
Volume 15, Issue 1, Pages -
Publisher
Springer Nature
Online
2014-09-15
DOI
10.1186/s12881-014-0099-0
References
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