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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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