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Human Molecular Genetics, Vol. 14, Iss. 2, 2005-01 ,pp. : 295-305

Oxford University Press

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Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

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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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Limb Girdle Muscular Dystrophy Type 2A (CAPN3): Mapping Using Allelic Association

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A slowly progressive form of limb‐girdle muscular dystrophy type 2C associated with founder mutation in the SGCG gene in Puerto Rican Hispanics

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John Wiley & Sons Inc

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