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Whole exome sequencing identifies a KCNJ12 mutation as a cause of familial dilated cardiomyopathy
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...
Shranjeno v:
| izdano v: | Medicine (Baltimore) |
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| Main Authors: | , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Wolters Kluwer Health
2017
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5571686/ https://ncbi.nlm.nih.gov/pubmed/28816949 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000007727 |
| Oznake: |
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