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• W2111462809 abstract "A mouse model for Duchenne muscular dystrophy engineered to produce human-like glycosylation mimics the human disease better than existing models." @default.
• W2111462809 created "2016-06-24" @default.
• W2111462809 creator A5017703428 @default.
• W2111462809 creator A5034630670 @default.
• W2111462809 creator A5036413821 @default.
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• W2111462809 creator A5064620149 @default.
• W2111462809 creator A5073313205 @default.
• W2111462809 creator A5083328627 @default.
• W2111462809 creator A5089853347 @default.
• W2111462809 date "2010-07-28" @default.
• W2111462809 modified "2023-10-12" @default.
• W2111462809 title "A Human-Specific Deletion in Mouse <i>Cmah</i> Increases Disease Severity in the mdx Model of Duchenne Muscular Dystrophy" @default.
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