Autosomal dominant cerebellar ataxia with deafness, myoclonus and amyotrophy.

Antzeko izenburuak

• Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological report.
  nork: Baraitser, M, et al.
  Argitaratua: (1984)
• Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy
  nork: Winkelmann, Juliane, et al.
  Argitaratua: (2012)
• Saccade velocity in idiopathic and autosomal dominant cerebellar ataxia.
  nork: Bürk, K, et al.
  Argitaratua: (1997)
• Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy
  nork: Kernohan, Kristin D., et al.
  Argitaratua: (2016)
• Genetic aspects of autosomal dominant late onset cerebellar ataxia.
  nork: Harding, A E
  Argitaratua: (1981)