Mitochondrial Energetics and Ca(2+)-Activated ATPase in Obstructive Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is the most common genetic disease of the myocardium associated to mutations in sarcomeric genes, but the link between genotype and phenotype remains poorly understood. Magnetic resonance spectroscopy studies have demonstrated impaired cardiac energetics in patients...

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Detalhes bibliográficos
Publicado no:J Clin Med
Main Authors: Lombardi, Maria, Lazzeroni, Davide, Pisano, Annalinda, Girolami, Francesca, Alfieri, Ottavio, La Canna, Giovanni, d’Amati, Giulia, Olivotto, Iacopo, Rimoldi, Ornella E., Foglieni, Chiara, Camici, Paolo G.
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7356244/
https://ncbi.nlm.nih.gov/pubmed/32527005
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm9061799
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