DataSet Record GDS3475: Expression Profiles Data Analysis Tools Sample Subsets
Title: Limb girdle muscular dystrophy 2A (HG-U133B)
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Summary: Analysis of skeletal muscles from patients with limb girdle muscular dystrophy 2A (LGMD2A). LGMD2A is a recessive genetic disorder caused by mutations in calpain 3 (CAPN3). Results provide insight into the molecular pathogenesis of LGMD2A.
Organism: Homo sapiens
Platform: GPL97: [HG-U133B] Affymetrix Human Genome U133B Array
Citation:
  • Sáenz A, Azpitarte M, Armañanzas R, Leturcq F et al. Gene expression profiling in limb-girdle muscular dystrophy 2A. PLoS One 2008;3(11):e3750. PMID: 19015733
Reference Series: GSE11681 Sample count: 17
Value type: transformed count Series published: 2008/11/18