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Full record GDS3474

Limb girdle muscular dystrophy 2A (HG-U133A)

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
Type:
Expression profiling by array, transformed count, 2 disease state sets
Platform:
GPL96
Series:
GSE11681
20 Samples
Download data:
GEO (CEL)

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