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- W2012806863 abstract "Duchenne muscular dystrophy (DMD) is the most common inherited human muscle disease and among the most debilitating. In recent investigations the locus of the gene in the Xp21 region of the X chromosome has been defined, the DMD gene has been cloned, and its protein product ‘dystrophin’ has been identified and partially characterized. The analysis of patterns of DMD gene and dystrophin defects in DMD and related disorders has provided insight into the molecular pathogenesis of differing clinical phenotypes of DMD. These studies have also identified two animal models homologous to human DMD. This review outlines these recent studies and their implications for understanding the molecular biology of DMD." @default.
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- W2012806863 date "1988-01-01" @default.
- W2012806863 modified "2023-10-16" @default.
- W2012806863 title "Molecular biology of Duchenne muscular dystrophy" @default.
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- W2012806863 doi "https://doi.org/10.1016/0166-2236(88)90006-9" @default.
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