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Identification of MYLK3 mutations in familial dilated cardiomyopathy
Dilated cardiomyopathy (DCM) is a primary cause of heart failure, life-threatening arrhythmias, and cardiac death. Pathogenic mutations have been identified at the loci of more than 50 genes in approximately 50% of DCM cases, while the etiologies of the remainder have yet to be determined. In this s...
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| Publicado en: | Sci Rep |
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| Autores principales: | , , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Nature Publishing Group UK
2017
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5727479/ https://ncbi.nlm.nih.gov/pubmed/29235529 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-17769-1 |
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