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The mdx mouse as a model for carnitine deficiency in the pathogenesis of duchenne muscular dystrophy

✍ Scribed by Zolkipli, Zarazuela; Mai, Lydia; Lamhonwah, Anne-Marie; Tein, Ingrid


Book ID
118764807
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
223 KB
Volume
46
Category
Article
ISSN
0148-639X

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The mdx mouse has a genetically homologous disease to Duchenne muscular dystrophy in humans. The disease progression, however, is not accompanied by the same level of fatty infiltration and muscle degeneration as occurs in humans. Thus, the presence of histological/ pathological changes in living md