## Abstract In the muscular dystrophic (mdx) mouse, which is characterized by deficient dystrophin expression and provides a model of Duchenne's muscular dystrophy, we previously demonstrated marked central nervous system alterations and in particular a quantitative reduction of corticospinal and r
β¦ LIBER β¦
Anionic phospholipids calcium binding sites in Duchenne and murine X-linked muscular dystrophy
β Scribed by Maurizio Moggio; Alessandro Prelle; Gigliola Fagiolari; Nicoletta Checcarelli; Monica Sciacco; Patrizia Ciscato; Guglielmo Scarlato
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 534 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0148-639X
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## Abstract Duchenne muscular dystrophy is an Xβlinked condition at the severe end of the spectrum of dystrophinopathies. Females with dystrophin mutations are at risk for cardiomyopathy, but are usually asymptomatic during childhood. However, some girls can exhibit features of Duchenne muscular dy
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