Cardiomyopathy is common in patients with the mitochondrial DNA m.3243A>G mutation and correlates with mutation load

Although neuromuscular clinical features often dominate the clinical presentation of mitochondrial disease due to the m.3243A>G mitochondrial DNA (mtDNA) mutation, many patients develop cardiac failure, which is often overlooked until it reaches an advanced stage. We set out to determine whether...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Hollingsworth, Kieren G., Gorman, Grainne S., Trenell, Michael I., McFarland, Robert, Taylor, Robert W., Turnbull, Douglass M., MacGowan, Guy A., Blamire, Andrew M., Chinnery, Patrick F.
Formato: Artigo
Idioma:Inglês
Publicado em: Pergamon Press 2012
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3387369/
https://ncbi.nlm.nih.gov/pubmed/22513320
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nmd.2012.03.001
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados