Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
Summary:
Analysis of muscle from 12 patients with various forms of mitochondrial encephalomyopathies associated with mitochondrial DNA mutations: 8 patients with a A3243G mutation, and 4 patients with a 4977 base pair deletion. Results identify possible expression signature for mitochondrial disorders.
GPL96:
[HG-U133A] Affymetrix Human Genome U133A Array
Citation:
Crimi M, Bordoni A, Menozzi G, Riva L et al. Skeletal muscle gene expression profiling in mitochondrial disorders. FASEB J 2005 May;19(7):866-8. PMID: 15728662
