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.
GPL81:
[MG_U74Av2] Affymetrix Murine Genome U74A Version 2 Array
Citation:
Sanoudou D, Corbett MA, Han M, Ghoddusi M et al. Skeletal muscle repair in a mouse model of nemaline myopathy. Hum Mol Genet 2006 Sep 1;15(17):2603-12. PMID: 16877500
