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http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_21/101093hmgddg307/authorship/9
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scienceplus.abes.fr
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http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_21/101093hmgddg307/affiliation/AF5
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Voit Thomas
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Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of α-dystroglycan
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