Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long-QT syndrome

Patient-specific induced pluripotent stem cells (iPSCs) will assist research on genetic cardiac maladies if the disease phenotype is recapitulated in vitro. However, genetic background variations may confound disease traits, especially for disorders with incomplete penetrance, such as long-QT syndro...

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Autors principals: Bellin, Milena, Casini, Simona, Davis, Richard P, D'Aniello, Cristina, Haas, Jessica, Ward-van Oostwaard, Dorien, Tertoolen, Leon G J, Jung, Christian B, Elliott, David A, Welling, Andrea, Laugwitz, Karl-Ludwig, Moretti, Alessandra, Mummery, Christine L
Format: Artigo
Idioma:Inglês
Publicat: European Molecular Biology Organization 2013
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3981141/
https://ncbi.nlm.nih.gov/pubmed/24213244
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/emboj.2013.240
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