Gene therapy of muscular dystrophy

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Oxford University Press

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The homeobox gene CHX10/VSX2 regulates RdCVF promoter activity in the inner retina

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Oxford University Press

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Homozygous Deletion Mutations in the Plectin Gene (PLEC1) in Patients with Epidermolysis Bullosa Simplex Associated with Late-Onset Muscular Dystrophy

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The Gene for Schnyder's Crystalline Corneal Dystrophy Maps to Human Chromosome 1p34.1–p36

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Human Molecular Genetics, Vol. 5, Iss. 10, 1996-10 ,pp. : 1667-1672

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Mutations in the retinal guanylate cyclase ( RETGC-1 ) gene in dominant cone–rod dystrophy

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Human Molecular Genetics, Vol. 7, Iss. 7, 1998-07 ,pp. : 1179-1184

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