GEO DataSets

Analysis of various skeletal muscles of trangenics expressing the human Met9Arg alpha-tropomyosin slow mutant gene, a model of nemaline myopathy (NM). NM, a non-dystrophic congenital myopathy, is a variably severe neuromuscular disorder. Results provide insight into the pathogenesis of NM.

Organism:

Mus musculus

Type:

Expression profiling by array, count, 2 age, 2 disease state, 5 tissue sets

Platform:

GPL81

Series:

GSE3384

36 Samples

Download data: CEL, EXP