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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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Autori principali: Magida, Jason A, Leinwand, Leslie A
Natura: Artigo
Lingua:Inglês
Pubblicazione: Backwell Publishing Ltd 2014
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3992075/
https://ncbi.nlm.nih.gov/pubmed/24567073
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/emmm.201302852
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