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Yoshihide Sunada

Howard Hughes Medical Institute

16

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1767

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β-Sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate

1998 Neuromuscular Disorders
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Mild Congenital Muscular Dystrophy in Two Patients with an Internally Deleted Laminin α2-Chain

1997 Human Molecular Genetics
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Dystroglycan Is Essential for Early Embryonic Development: Disruption of Reichert's Membrane in Dag1-Null Mice

1997 Human Molecular Genetics
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Absence of γ‐sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12

1996 FEBS Letters
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From adhalinopathies to alpha-sarcoglycanopathies: An overview

1996 Neuromuscular Disorders
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Identification of muscle-specific calpain and β-sarcoglycan genes in progressive autosomal recessive muscular dystrophies

1996 Neuromuscular Disorders
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Citations (8)
Characterization of δ-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy

1996 Journal of Biological Chemistry
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Clinical heterogeneity of adhalin deficiency

1996 Annals of Neurology
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Muscular dystrophy associated with β-dystroglycan deficiency

1996 Annals of Neurology
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Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy

1995 Human Molecular Genetics
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Citations (141)