A Novel Missense Mutation in the Spectrin Beta Nonerythrocytic 2 Gene Likely Associated with Spinocerebellar Ataxia Type 5

مواد مشابهة

• A Family with Spinocerebellar Ataxia Type 5 Found to Have a Novel Missense Mutation Within a SPTBN2 Spectrin Repeat
  بواسطة: Cho, Ellen, وآخرون
  منشور في: (2013)
• Spectrin mutations that cause spinocerebellar ataxia type 5 impair axonal transport and induce neurodegeneration in Drosophila
  بواسطة: Lorenzo, Damaris N., وآخرون
  منشور في: (2010)
• Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia
  بواسطة: Huang, Lijia, وآخرون
  منشور في: (2012)
• Metabolic Profiling Reveals Biochemical Pathways and Potential Biomarkers of Spinocerebellar Ataxia 3
  بواسطة: Yang, Zhi-hua, وآخرون
  منشور في: (2019)
• Missense Mutation in CAPN1 Is Associated with Spinocerebellar Ataxia in the Parson Russell Terrier Dog Breed
  بواسطة: Forman, Oliver P., وآخرون
  منشور في: (2013)