Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G

Ítems similars

• Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.
  per: Majamaa, K, et al.
  Publicat: (1998)
• Mitochondrial DNA deletion diagnosed by analysis of an endomyocardial biopsy specimen from a patient with Kearns-Sayre syndrome and complete heart block
  per: Remes, Anne M, et al.
  Publicat: (1992)
• Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers
  per: Weiduschat, Nora, et al.
  Publicat: (2014)
• Cognitive impairment profile in patients with the m.3243A> G variant in mitochondrial DNA
  per: Satu Winqvist, et al.
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• m.3243A>G Mutation in Mitochondrial DNA Leads to Decreased Insulin Sensitivity in Skeletal Muscle and to Progressive β-Cell Dysfunction
  per: Lindroos, Markus M., et al.
  Publicat: (2009)