Slow-progressive ataxia with a methionine-to-arginine point mutation in codon 232 in the prion protein gene (PRNP)

Yoshinori Nishimoto, Daisuke Ito, Shigeaki Suzuki, Toshihiko Shimizu, Tetsuyuki Kitamoto, Norihiro Suzuki

Research output: Contribution to journalArticle

1 Citation (Scopus)
Original languageEnglish
Pages (from-to)696-698
Number of pages3
JournalClinical Neurology and Neurosurgery
Volume113
Issue number8
DOIs
Publication statusPublished - 2011 Oct

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Cerebellar Ataxia
Cerebral Angiography
Creutzfeldt-Jakob Syndrome
Magnetic Resonance Angiography
Prions
Vision Disorders
Ataxia
Single-Photon Emission-Computed Tomography
Point Mutation
Codon
Methionine
Arginine
Electroencephalography
Magnetic Resonance Imaging
Genes
Prion Proteins

Keywords

  • Creutzfeldt-Jakob disease
  • M232R
  • Prion protein gene
  • Valine/methionine variant

ASJC Scopus subject areas

  • Clinical Neurology
  • Surgery

Cite this

Slow-progressive ataxia with a methionine-to-arginine point mutation in codon 232 in the prion protein gene (PRNP). / Nishimoto, Yoshinori; Ito, Daisuke; Suzuki, Shigeaki; Shimizu, Toshihiko; Kitamoto, Tetsuyuki; Suzuki, Norihiro.

In: Clinical Neurology and Neurosurgery, Vol. 113, No. 8, 10.2011, p. 696-698.

Research output: Contribution to journalArticle

Nishimoto, Yoshinori ; Ito, Daisuke ; Suzuki, Shigeaki ; Shimizu, Toshihiko ; Kitamoto, Tetsuyuki ; Suzuki, Norihiro. / Slow-progressive ataxia with a methionine-to-arginine point mutation in codon 232 in the prion protein gene (PRNP). In: Clinical Neurology and Neurosurgery. 2011 ; Vol. 113, No. 8. pp. 696-698.
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