Autosomal recessive late onset multisystem disorder with cerebellar cortical atrophy at necropsy: report of a family.

Samankaltaisia teoksia

• AMACR mutations cause late-onset autosomal recessive cerebellar ataxia
  Tekijä: Dick, David, et al.
  Julkaistu: (2011)
• Genetic aspects of autosomal dominant late onset cerebellar ataxia.
  Tekijä: Harding, A E
  Julkaistu: (1981)
• Comparing cortical signatures of atrophy between late-onset and autosomal dominant Alzheimer disease
  Tekijä: Dincer, Aylin, et al.
  Julkaistu: (2020)
• Late-onset autosomal recessive cerebellar ataxia and neuropathy with a novel splicing mutation in the ATM gene
  Tekijä: Haruo Shimazaki, Junya Kobayashi, Ryo Sugaya, Imaharu Nakano, Shigeru Fujimoto
  Julkaistu: (2020-03-01)
• Delayed Cortical Cerebellar Atrophy. ? Familial Tremor
  Tekijä: Pritchard, E. A. Blake
  Julkaistu: (1934)