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A multiplex PCR strategy to screen for known mutations in families with sudden cardiac death burden
Ventricular tachyarrythmia occurring in ischemic heart disease, dilated/hypertrophic cardiomyopathies or rare monogenic mutations of cardiac ion channels or associated proteins belong to the most frequent causes of sudden cardiac death (SCD). In further decades, next generation sequencing and bioinf...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Journal of Biological Methods
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706106/ https://www.ncbi.nlm.nih.gov/pubmed/31453232 http://dx.doi.org/10.14440/jbm.2017.181 |