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...

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Detalles Bibliográficos
Autores principales: Duong, Giang, Helms, Thomas M., Karle, Christoph A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Journal of Biological Methods 2017
Materias:
Article
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

Internet

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

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