Article
Genetic aspects of the oxidative phosphorylation dysfunction in dilated cardiomyopathy.
Mutation research. Reviews in mutation research - 1 Jan 2000
Bayona-Bafaluy M Pilar, Iglesias Eldris, López-Gallardo Ester, Emperador Sonia, Pacheu-Grau David, Labarta Lorenzo, Montoya Julio, Ruiz-Pesini Eduardo
Abstract excerpt
Dilated cardiomyopathy is a frequent and extremely heterogeneous medical condition. Deficits in the oxidative phosphorylation system have been described in patients suffering from dilated cardiomyopathy. Hence, mutations in proteins related to this biochemical pathway could be etiological factors for some of these patients. Here, we review the clinical phenotypes of patients harboring pathological mutations in...
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