Mutation-Specific Phenotypes in hiPSC-Derived Cardiomyocytes Carrying Either Myosin-Binding Protein C Or α-Tropomyosin Mutation for Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is a genetic cardiac disease, which affects the structure of heart muscle tissue. The clinical symptoms include arrhythmias, progressive heart failure, and even sudden cardiac death but the mutation carrier can also be totally asymptomatic. To date, over 1400 mutati...

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Detalhes bibliográficos
Publicado no:Stem Cells Int
Main Authors: Ojala, Marisa, Prajapati, Chandra, Pölönen, Risto-Pekka, Rajala, Kristiina, Pekkanen-Mattila, Mari, Rasku, Jyrki, Larsson, Kim, Aalto-Setälä, Katriina
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2016
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4707351/
https://ncbi.nlm.nih.gov/pubmed/27057166
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/1684792
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