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.
GPL96:
[HG-U133A] Affymetrix Human Genome U133A 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