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Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution

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Year: 2007
Type: article
Study design: Observational Study
Source: Journal of Neurology
DOI: 10.1007/s00415-007-0540-9
Authors: Y. Shiga*, K. Satoh, T. Kitamoto*, S. Kanno, I. Nakashima, S. Sato, K. Fujihara, H. Takata, K. Nobukuni, S. Kuroda*, H. Takano, Y. Umeda, H. Konno, K. Nagasato, A. Satoh, Y. Matsuda, M. Hidaka, H. Takahashi, Y. Sano, K. Kim, T. Konishi, K. Doh-ura, T. Sato*, K. Sasaki, Y. Nakamura*, M. Yamada*, H. Mizusawa*, Y. Itoyama
Institutions: Tohoku University, Nagasaki University, Kohnan Hospital, Okayama University, Brain Research Institute, Niigata University, Niigata University, Sendai Nishitaga National Hospital, Isahaya General Hospital, Yamaguchi University, Matsudo City Hospital, Shizuoka General Hospital, Shizuoka Medical Center, National Center of Neurology and Psychiatry, Kohnodai Hospital, National Center for Global Health and Medicine, Kyushu University, Neurological Institute, Graduate School of Medical Sciences, Kyushu University, Jichi Medical University, Kanazawa University, Tokyo Medical and Dental University
Language: English

Topic: Prion Diseases and Protein Misfolding
Subfield: Molecular Biology
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W2017187408
FWCI: 0.979
Cites: 32
Cited by: 45
Related to: 10
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