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
Pages (from-to)388
Number of pages1
JournalJournal of Neurology Neurosurgery and Psychiatry
Volume68
Issue number3
DOIs
Publication statusPublished - 2000

ASJC Scopus subject areas

  • Surgery
  • Clinical Neurology
  • Psychiatry and Mental health

Cite this

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. (2000). Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia. Journal of Neurology Neurosurgery and Psychiatry, 68(3), 388. https://doi.org/10.1136/jnnp.68.3.388