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January 10, 2013Neurology

Mutations in the gene encoding p62 in Japanese patients with amyotrophic lateral sclerosis

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Authors

MHMakito HiranoKindai UniversityYNYusaku NakamuraOsaka Prefectural Medical CenterKSKazumasa SaigohKindai University Hospital

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Hirano et al. (2013) studied this question.

synapsesocial.com/papers/6a7f37d1b5ccfbbe2d84ef3dhttps://doi.org/10.1212/wnl.0b013e31827f0fe5
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Also Consider

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

  1. 1SQSTM1 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis2011 · 659 citations
  2. 2PMUT: a web-based tool for the annotation of pathological mutations on proteins2005 · 506 citations
  3. 3A Novel Mutation (K378X) in the Sequestosome 1 Gene Associated With Increased NF-κB Signaling and Paget's Disease of Bone With a Severe Phenotype2006 · 94 citations