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- W2284966626 abstract "With the discovery of the X-linked gene product dystrophin, the mdx mouse came to be regarded as the only suitable mouse model of human muscular dystrophy. However, existence of an autosomal gene homologous with dystrophin, together with physiological evidence of membrane fragility, reestablishes autosomal mouse mutants (dy, dy2j) as valid models." @default.
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- W2284966626 date "1992-10-01" @default.
- W2284966626 modified "2023-10-06" @default.
- W2284966626 title "Mouse Models of Muscular Dystrophy: Gene Products and Function" @default.
- W2284966626 doi "https://doi.org/10.1152/physiologyonline.1992.7.5.195" @default.
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