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FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy
A genetic etiology has been identified in 30% to 40% of dilated cardiomyopathy (DCM) patients, yet only 50% of these cases are associated with a known causative gene variant. Thus, in order to understand the pathophysiology of DCM, it is necessary to identify and characterize additional genes. In th...
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| Publicado no: | JACC Basic Transl Sci |
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| Main Authors: | , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5166708/ https://ncbi.nlm.nih.gov/pubmed/28008423 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jacbts.2016.05.004 |
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