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

doi:10.1136/jnnp.68.3.388

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

研究成果: Letter › 査読

31 被引用数 (Scopus)

本文言語	English
ページ（範囲）	388
ページ数	1
ジャーナル	Journal of Neurology Neurosurgery and Psychiatry
巻	68
号	3
DOI	https://doi.org/10.1136/jnnp.68.3.388
出版ステータス	Published - 2000
外部発表	はい

ASJC Scopus subject areas

外科
臨床神経学
精神医学および精神衛生

UN SDG

この成果は、次の持続可能な開発目標に貢献しています

文献へのアクセス

10.1136/jnnp.68.3.388

他のファイルとリンク

引用スタイル

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

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, vol. 68, no. 3, pp. 388. https://doi.org/10.1136/jnnp.68.3.388

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AU - Hara, H.

AU - Doh-Ura, K.

AU - Murakami, I.

AU - Tashiro, H.

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AU - Shigeto, H.

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AU - Araki, E.

AU - Yamada, T.

AU - Iwaki, T.

AU - Kira, J.

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