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- W3119461552 endingPage "558" @default.
- W3119461552 startingPage "558" @default.
- W3119461552 abstract "The sarcomere as the smallest contractile unit is prone to alterations in its functional, structural and associated proteins. Sarcomeric dysfunction leads to heart failure or cardiomyopathies like hypertrophic (HCM) or restrictive cardiomyopathy (RCM) etc. Genetic based RCM, a very rare but severe disease with a high mortality rate, might be induced by mutations in genes of non-sarcomeric, sarcomeric and sarcomere associated proteins. In this review, we discuss the functional effects in correlation to the phenotype and present an integrated model for the development of genetic RCM." @default.
- W3119461552 created "2021-01-18" @default.
- W3119461552 creator A5012543949 @default.
- W3119461552 creator A5026145133 @default.
- W3119461552 creator A5043451845 @default.
- W3119461552 creator A5087473504 @default.
- W3119461552 date "2021-01-08" @default.
- W3119461552 modified "2023-10-15" @default.
- W3119461552 title "Genetic Restrictive Cardiomyopathy: Causes and Consequences—An Integrative Approach" @default.
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