Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factor

Brain

Volumn 120, Issue 3, 1997, Pages 491-501

  Fox, N C ^a,b   Kennedy, A M ^a   Harvey, R J ^a,b   Lantos, P L ^c   Roques, P K ^a   Collinge, J ^b   Hardy, J ^d   Hutton, M ^b   Stevens, J M ^a,b   Warrington, E K ^a   Rossor, M N ^a,b  

^a NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

^b IMPERIAL COLLEGE SCHOOL OF MEDICINE   (United Kingdom)

^c KING'S COLLEGE LONDON   (United Kingdom)

^d UNIVERSITY OF SOUTH FLORIDA   (United States)

Author keywords

Age at onset; Alzheimer's disease; Chromosome 14; Early onset; Familial; Presenilin

Indexed keywords

ADULT; ALZHEIMER DISEASE; AMNESIA; ARTICLE; CHROMOSOME 14; COGNITION; GENE; GENE LOCATION; HUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; VERBAL MEMORY;

ADULT; ALZHEIMER DISEASE; APOLIPOPROTEINS E; BRAIN; FEMALE; HUMANS; INTELLIGENCE; MALE; MEMORY; MIDDLE AGED; MUTATION; NEUROPSYCHOLOGICAL TESTS; PEDIGREE; PERCEPTION;

EID: 0030944258     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/120.3.491     Document Type: Article

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