Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation

Neurology

Volumn 55, Issue 10, 2000, Pages 1577-1578

  Raux, G ^a   Gantier, R ^a   Thomas Anterion, C ^b   Boulliat, J ^c   Verpillat, P ^a   Hannequin, D ^a   Brice, A ^a   Frebourg, T ^a   Campion, D ^a  

^a INSERM   (France)

^b SERVICE DE NEUROLOGIE   (France)

^c CHR Bourg en Bresse   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PRESENILIN 1;

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BRAIN MAPPING; CASE REPORT; CHROMOSOME 17Q; CLINICAL FEATURE; DEMENTIA; FEMALE; FRONTAL LOBE; GENE LOCATION; GENE MUTATION; HUMAN; MULTIGENE FAMILY; PRIORITY JOURNAL; SEQUENCE ANALYSIS; TEMPORAL LOBE;

EID: 0034727610     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.55.10.1577     Document Type: Article

References (9)

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4. Tau is a candidate gene for chromosome 17 frontotemporal dementia
5. Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism
6. Clinical and neuropathological criteria for frontotemporal dementia
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8. A study of the Lund-Manchester research criteria for frontotemporal dementia: Clinical and single photon emission CT correlations
9. Clinical and pathological evidences for a frontal variant of Alzheimer's disease