Cell surface and gene expression regulation molecules in dystrophinopathy: mdx vs. Duchenne
Duchenne muscular dystrophy (DMD) is secondary to loss-of-function mutations in the dystrophin gene. The causes underlying the progression of DMD, differential muscle involvement, and the discrepancies in phenotypes among species with the same genetic defect are not understood. The mdx mouse, an ani...
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| Lenguaje: | English |
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Sociedad de Biología de Chile
2005
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| Acceso en línea: | http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602005000400010 |
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