DataSet Record GDS1065: Expression Profiles Data Analysis Tools Sample Subsets
Title: Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
Cluster AnalysisGDS1065 Cluster Image
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.
Organism: Homo sapiens
Platform: GPL96: [HG-U133A] Affymetrix Human Genome U133A Array
  • 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
Reference Series: GSE1462 Sample count: 15
Value type: count Series published: 2005/01/22