(Q33688704)
Statements
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An inherited prion disease with a PrP P105L mutation: clinicopathologic and PrP heterogeneity (English)
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Yamada M
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Itoh Y
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Inaba A
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Wada Y
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Takashima M
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Satoh S
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Kamata T
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Okeda R
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Kayano T
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Suematsu N
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Kitamoto T
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Otomo E
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Matsushita M
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Mizusawa H
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1 July 1999
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53
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181-188
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Identifiers
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