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Full record GDS3475

Limb girdle muscular dystrophy 2A (HG-U133B)

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:
GPL97
Series:
GSE11681
17 Samples
Download data: CEL
DataSet
Accession:
GDS3475
ID:
3475

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