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A case of Creutzfeldt-Jakob disease with a novel insertion mutation and codon 219 Lysine/Lysine polymorphism in the prion protein gene

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Prions

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Author information

Authors and Affiliations

  1. The Department of Neurology and Neurological Science, Graduate School, Tokyo Medical and Dental University, Tokyo, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan

    Y. Nishida, N. Sodeyama, Y. Toru, S. Toru & H. Mizusawa

  2. Department of Neurological Science, Tohoku University, School of Medicine, Japan

    T. Kitamoto

Authors
  1. Y. Nishida
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  2. N. Sodeyama
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  3. Y. Toru
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  4. S. Toru
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  5. T. Kitamoto
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  6. H. Mizusawa
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Editor information

Editors and Affiliations

  1. Department of Prion Research, Tohoku University School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai, 980-8575, Japan

    Tetsuyuki Kitamoto M.D.

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© 2005 Springer-Verlag Tokyo

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Nishida, Y., Sodeyama, N., Toru, Y., Toru, S., Kitamoto, T., Mizusawa, H. (2005). A case of Creutzfeldt-Jakob disease with a novel insertion mutation and codon 219 Lysine/Lysine polymorphism in the prion protein gene. In: Kitamoto, T. (eds) Prions. Springer, Tokyo. https://doi.org/10.1007/4-431-29402-3_52

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  • DOI: https://doi.org/10.1007/4-431-29402-3_52

  • Publisher Name: Springer, Tokyo

  • Print ISBN: 978-4-431-25539-0

  • Online ISBN: 978-4-431-29402-3

  • eBook Packages: MedicineMedicine (R0)

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