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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Udgivet i:Stem Cells Int
Main Authors: Ojala, Marisa, Prajapati, Chandra, Pölönen, Risto-Pekka, Rajala, Kristiina, Pekkanen-Mattila, Mari, Rasku, Jyrki, Larsson, Kim, Aalto-Setälä, Katriina
Format: Artigo
Sprog:Inglês
Udgivet: Hindawi Publishing Corporation 2016
Fag:
Research Article
Online adgang: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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