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Functional muscle ischemia in neuronal nitric oxide synthase-deficient skeletal muscle of children with Duchenne muscular dystrophy

Duchenne muscular dystrophy (DMD) is a fatal disease caused by mutation of the gene encoding the cytoskeletal protein dystrophin. Despite a wealth of recent information about the molecular basis of DMD, effective treatment for this disease does not exist because the mechanism by which dystrophin def...

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Autors principals: Sander, Mikael, Chavoshan, Bahman, Harris, Shannon A., Iannaccone, Susan T., Stull, James T., Thomas, Gail D., Victor, Ronald G.
Format: Artigo
Idioma:Inglês
Publicat: The National Academy of Sciences 2000
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC17659/
https://ncbi.nlm.nih.gov/pubmed/11087833
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