Generation of two iPSC lines from long QT syndrome patients carrying SNTA1 variants

Long QT syndrome (LQTS) is an inherited cardiovascular disorder characterized by electrical conduction abnormalities leading to arrhythmia, fainting, seizures, and an increased risk of sudden death. There are over 15 genes involved in causing LQTS, including SNTA1. Here we generated two human-induce...

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Detalles Bibliográficos
Autores principales: Jimenez-Tellez, Nerea, Vera, Carlos D., Yildirim, Zehra, Guevara, Julio Vicente, Zhang, Tina, Wu, Joseph C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10029814/
https://www.ncbi.nlm.nih.gov/pubmed/36528013
http://dx.doi.org/10.1016/j.scr.2022.103003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10029814/
https://www.ncbi.nlm.nih.gov/pubmed/36528013
http://dx.doi.org/10.1016/j.scr.2022.103003

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