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December 26, 2000Neurology

Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy

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Authors

СИС. Н. ИллариошкинMoscow State University of Medicine and DentistryIII. A. Ivanova‐SmolenskayaAcademy of Medical SciencesCGCheryl R. GreenbergManitoba Health

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Иллариошкин et al. (2000) studied this question.

synapsesocial.com/papers/6a090a3562c780efd627fcaehttps://doi.org/10.1212/wnl.55.12.1931
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Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Identical Mutation in Patients with Limb Girdle Muscular Dystrophy Type 2B Or Miyoshi Myopathy Suggests a Role for Modifier Gene(s)1999 · 182 citations
  2. 2A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p1994 · 195 citations
  3. 3Three years' experience with neonatal screening for Duchenne/Becker Muscular dystrophy: Gene analysis, gene expression, and phenotype prediction1991 · 27 citations