Whole exome sequencing identifies a KCNJ12 mutation as a cause of familial dilated cardiomyopathy
Abstract
Dilated cardiomyopathy (DCM) is characterized by left ventricular dilation, and is associated with systolic dysfunction and increased action potential duration. Approximately 50% of DCM cases are caused by inherited gene mutations with genetic and phenotypic heterogeneity. Next generation sequencing may be useful in screening unknown mutations in such cases. A family was identified with DCM, in which the affected family members developed heart...
Paper Details
Title
Whole exome sequencing identifies a KCNJ12 mutation as a cause of familial dilated cardiomyopathy
Published Date
Aug 1, 2017
Journal
Volume
96
Issue
33
Pages
e7727 - e7727
Citation AnalysisPro
You’ll need to upgrade your plan to Pro
Looking to understand the true influence of a researcher’s work across journals & affiliations?
- Scinapse’s Top 10 Citation Journals & Affiliations graph reveals the quality and authenticity of citations received by a paper.
- Discover whether citations have been inflated due to self-citations, or if citations include institutional bias.
Notes
History