Allele-specific RNA interference rescues the long-QT syndrome phenotype in human-induced pluripotency stem cell cardiomyocytes

AIMS: Long-QT syndromes (LQTS) are mostly autosomal-dominant congenital disorders associated with a 1:1000 mutation frequency, cardiac arrest, and sudden death. We sought to use cardiomyocytes derived from human-induced pluripotency stem cells (hiPSCs) as an in vitro model to develop and evaluate ge...

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Detalles Bibliográficos
Autores principales: Matsa, Elena, Dixon, James E., Medway, Christopher, Georgiou, Orestis, Patel, Minal J., Morgan, Kevin, Kemp, Paul J., Staniforth, Andrew, Mellor, Ian, Denning, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Basic Science
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992427/
https://www.ncbi.nlm.nih.gov/pubmed/23470493
http://dx.doi.org/10.1093/eurheartj/eht067

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992427/
https://www.ncbi.nlm.nih.gov/pubmed/23470493
http://dx.doi.org/10.1093/eurheartj/eht067

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