Generation of two iPSC lines from hypertrophic cardiomyopathy patients carrying MYBPC3 and PRKAG2 variants

Hypertrophic cardiomyopathy (HCM) is an inherited cardiac disorder characterized by a thick left ventricular wall and an increased risk of arrhythmias, heart failure, and sudden cardiac death. The MYBPC3 and PRAKG2 are known causal genes for HCM. Here we generated two human-induced pluripotent stem...

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Detalles Bibliográficos
Autores principales: Manhas, Amit, Jahng, James W.S., Vera, Carlos D., Shenoy, Sushma P., Knowles, Joshua W., Wu, Joseph C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708393/
https://www.ncbi.nlm.nih.gov/pubmed/35413566
http://dx.doi.org/10.1016/j.scr.2022.102774

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708393/
https://www.ncbi.nlm.nih.gov/pubmed/35413566
http://dx.doi.org/10.1016/j.scr.2022.102774

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