An inherited prion disease with a PrP P105L mutation: Clinicopathologic and PrP heterogeneity

Neurology

Volumn 53, Issue 1, 1999, Pages 181-188

  Yamada, M ^a   Itoh, Y ^b   Inaba, A ^a   Wada, Y ^a   Takashima, M ^a   Satoh, S ^a   Kamata, T ^a   Okeda, R ^a   Kayano, T ^a   Suematsu, N ^b   Kitamoto, T ^c   Otomo, E ^b   Matsushita, M ^c   Mizusawa, H ^a  

^a TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

^b Yokufukai Geriatric Hospital   (Japan)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

PRION PROTEIN;

ADULT; ARTICLE; ATAXIA; CASE REPORT; CLINICAL EXAMINATION; DEMENTIA; DNA POLYMORPHISM; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; IMMUNOBLOTTING; IMMUNOHISTOCHEMISTRY; JAPAN; MALE; MYOCLONUS; NEUROFIBRILLARY TANGLE; NEUROPATHOLOGY; PRION DISEASE; PRIORITY JOURNAL; SIBLING; SPASTIC PARESIS;

EID: 0033551458     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.53.1.181     Document Type: Article

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