Genetic aspects of autosomal dominant late onset cerebellar ataxia.

Παρόμοια τεκμήρια

• Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological report.
  ανά: Baraitser, M, κ.ά.
  Έκδοση: (1984)
• Late onset autosomal dominant cerebellar ataxia a family description and linkage analysis with the hla system
  ανά: Walter O. Arruda, κ.ά.
  Έκδοση: (1991-09-01)
• Early onset cerebellar ataxia with retained tendon reflexes: a clinical and genetic study of a disorder distinct from Friedreich's ataxia.
  ανά: Harding, A E
  Έκδοση: (1981)
• AMACR mutations cause late-onset autosomal recessive cerebellar ataxia
  ανά: Dick, David, κ.ά.
  Έκδοση: (2011)
• AB065. Genetic testing and counseling in family with late onset autosomal dominant spinocerebellar ataxia
  ανά: Listyasari, Nurin Aisyiyah, κ.ά.
  Έκδοση: (2017)