Inherited prion encephalopathy associated with the novel PRNP H187R mutation: A clinical study

Neurology

Volumn 55, Issue 4, 2000, Pages 517-522

  Butefisch C M ^a   Gambetti, P ^c   Cervenakova, L ^b   Park, K Y ^a   Hallett, M ^a   Goldfarb, L G ^a,d  

^a NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

^b HOLLAND LABORATORY   (United States)

^c CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PRION PROTEIN;

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BRAIN BIOPSY; BRAIN DISEASE; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE DURATION; FEMALE; GENE MUTATION; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IMAGE ANALYSIS; MALE; ONSET AGE; PRION DISEASE; PRIORITY JOURNAL;

EID: 0033845973     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.55.4.517     Document Type: Article

References (20)

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