Welander hereditary distal myopathy, a molecular genetic comparison to hereditary myopathies with inclusion bodies
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Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/ limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13
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A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
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Distribution of muscle degeneration in Welander distal myopathy a magnetic resonance imaging and muscle biopsy study
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Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s)
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