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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356244/
https://www.ncbi.nlm.nih.gov/pubmed/32527005
http://dx.doi.org/10.3390/jcm9061799

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356244/
https://www.ncbi.nlm.nih.gov/pubmed/32527005
http://dx.doi.org/10.3390/jcm9061799

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