Deciphering Common Long QT Syndrome Using CRISPR/Cas9 in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes

From carrying potentially pathogenic genes to severe clinical phenotypes, the basic research in the inherited cardiac ion channel disease such as long QT syndrome (LQTS) has been a significant challenge in explaining gene-phenotype heterogeneity. These have opened up new pathways following the paral...

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Detalles Bibliográficos
Autores principales: Song, Yongfei, Zheng, Zequn, Lian, Jiangfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136094/
https://www.ncbi.nlm.nih.gov/pubmed/35647048
http://dx.doi.org/10.3389/fcvm.2022.889519

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136094/
https://www.ncbi.nlm.nih.gov/pubmed/35647048
http://dx.doi.org/10.3389/fcvm.2022.889519

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