Novel Autosomal Recessive c10orf2 Mutations Causing Infantile-Onset Spinocerebellar Ataxia

Podobne zapisy

• Novel Autosomal Recessive c10orf2 Mutations Causing Infantile-Onset Spinocerebellar Ataxia
  od: Jessica N. Hartley, i wsp.
  Wydane: (2012-01-01)
• Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy
  od: Park, Mi-Hyun, i wsp.
  Wydane: (2014)
• Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive disease
  od: Pierce, Sarah B., i wsp.
  Wydane: (2016)
• Autosomal Dominant Spinocerebellar Ataxia
  od: Shakkottai, Vikram G., i wsp.
  Wydane: (2013)
• Autosomal Recessive Spinocerebellar Ataxia Caused by a Novel Homozygous ANO10 Mutation in a Consanguineous Chinese Family
  od: Yang, Shi-Lin, i wsp.
  Wydane: (2020)