Metabolic crosstalk between the heart and liver impacts familial hypertrophic cardiomyopathy

Familial hypertrophic cardiomyopathy (HCM) is largely caused by dominant mutations in genes encoding cardiac sarcomeric proteins, and it is etiologically distinct from secondary cardiomyopathies resulting from pressure/volume overload and neurohormonal or inflammatory stimuli. Here, we demonstrate t...

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Detalles Bibliográficos
Autores principales: Magida, Jason A, Leinwand, Leslie A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Backwell Publishing Ltd 2014
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992075/
https://www.ncbi.nlm.nih.gov/pubmed/24567073
http://dx.doi.org/10.1002/emmm.201302852

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992075/
https://www.ncbi.nlm.nih.gov/pubmed/24567073
http://dx.doi.org/10.1002/emmm.201302852

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