Novel Autosomal Recessive c10orf2 Mutations Causing Infantile-Onset Spinocerebellar Ataxia

Antzeko izenburuak

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