Novel Autosomal Recessive c10orf2 Mutations Causing Infantile-Onset Spinocerebellar Ataxia

Παρόμοια τεκμήρια

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