Article ID Journal Published Year Pages File Type
10764337 Biochemical and Biophysical Research Communications 2010 5 Pages PDF
Abstract
► Wide phenotypic heterogeneity exists with mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome. ► We expand the phenotype of MELAS syndrome associated with the 3260A > G mutation to include cardiomyopathy, exercise-induced hearing loss, exercise-induced rhabdomyolysis, and autism. ► This phenotypic variability is not race-specific, as previously hypothesized.
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