Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia

Y. Taniwaki, H. Hara, K. Doh-Ura, I. Murakami, H. Tashiro, T. Yamasaki, H. Shigeto, K. Arakawa, E. Araki, T. Yamada, T. Iwaki, J. Kira

Research output: Contribution to journalLetter

29 Citations (Scopus)
Original languageEnglish
Number of pages1
JournalJournal of Neurology Neurosurgery and Psychiatry
Volume68
Issue number3
DOIs
Publication statusPublished - May 19 2000

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Cerebellar Ataxia
Creutzfeldt-Jakob Syndrome
Protein Precursors
Prions
Sleep Initiation and Maintenance Disorders
Pedigree
Amyloid
Differential Diagnosis
Genotype
Mutation

All Science Journal Classification (ASJC) codes

  • Surgery
  • Clinical Neurology
  • Psychiatry and Mental health

Cite this

Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia. / Taniwaki, Y.; Hara, H.; Doh-Ura, K.; Murakami, I.; Tashiro, H.; Yamasaki, T.; Shigeto, H.; Arakawa, K.; Araki, E.; Yamada, T.; Iwaki, T.; Kira, J.

In: Journal of Neurology Neurosurgery and Psychiatry, Vol. 68, No. 3, 19.05.2000.

Research output: Contribution to journalLetter

Taniwaki, Y. ; Hara, H. ; Doh-Ura, K. ; Murakami, I. ; Tashiro, H. ; Yamasaki, T. ; Shigeto, H. ; Arakawa, K. ; Araki, E. ; Yamada, T. ; Iwaki, T. ; Kira, J. / Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia. In: Journal of Neurology Neurosurgery and Psychiatry. 2000 ; Vol. 68, No. 3.
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AU - Murakami, I.

AU - Tashiro, H.

AU - Yamasaki, T.

AU - Shigeto, H.

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AU - Araki, E.

AU - Yamada, T.

AU - Iwaki, T.

AU - Kira, J.

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