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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Bibliographische Detailangaben
Veröffentlicht in:Stem Cells Int
Hauptverfasser: Ojala, Marisa, Prajapati, Chandra, Pölönen, Risto-Pekka, Rajala, Kristiina, Pekkanen-Mattila, Mari, Rasku, Jyrki, Larsson, Kim, Aalto-Setälä, Katriina
Format: Artigo
Sprache:Inglês
Veröffentlicht: Hindawi Publishing Corporation 2016
Schlagworte:
Research Article
Online Zugang: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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