PRNP H187R mutation associated with neuropsychiatric disorders in childhood and dementia

Neurology

Volumn 64, Issue 7, 2005, Pages 1304-1306

  Hall, D A ^a,b   Leehey, M A ^a,b   Filley, C M ^a,b   Steinbart, E ^d   Montine, T ^d   Schellenberg, G D ^b,d   Bosque, P ^a,c   Nixon, R ^e   Bird, T ^b,d  

^a UNIVERSITY OF COLORADO   (United States)

^b VETERANS AFFAIRS MEDICAL CENTER   (United States)

^c DENVER HEALTH MEDICAL CENTER   (United States)

^d UNIVERSITY OF WASHINGTON   (United States)

^e OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PHENYTOIN; PRION PROTEIN;

ADULT; AGGRESSION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAIN ATROPHY; CHILD; CHILDHOOD DISEASE; CLINICAL ARTICLE; COMPUTER ASSISTED TOMOGRAPHY; DEMENTIA; DEVELOPMENTAL DISORDER; DYSLEXIA; ELECTROENCEPHALOGRAM; FEMALE; GENE; GENE MUTATION; GLIOSIS; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; IMPULSIVENESS; KLEPTOMANIA; MALE; MENTAL DISEASE; NEUROLOGIC DISEASE; NEUROPATHOLOGY; NEUROPSYCHOLOGICAL TEST; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PEDIGREE ANALYSIS; PEDOPHILIA; PRION DISEASE; PRIORITY JOURNAL; PRNP GENE; PSYCHOSIS; PYROMANIA; SEIZURE; SYMPTOMATOLOGY;

EID: 16844366145     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000156911.70131.06     Document Type: Article

References (8)

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