Genotype-phenotype correlation in early-onset Alzheimer disease with presenilin 1 gone mutations

被引:7
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Larner, AJ
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10.1001/archneur.61.5.801-a
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R74 [神经病学与精神病学];
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页码:801 / 801
页数:1
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[1]  
HANISCH F, 2003, J NEUROL S2, V250, P98
[2]   Early-onset Alzheimer's disease with presenilin-1 M139V mutation: clinical, neuropsychological and neuropathological study [J].
Larner, AJ ;
du Plessis, DG .
EUROPEAN JOURNAL OF NEUROLOGY, 2003, 10 (03) :319-323
[3]   A novel mutation (V89L) in the presenilin 1 gene in a family with early onset Alzheimer's disease and marked behavioural disturbances [J].
Queralt, R ;
Ezquerra, M ;
Lleó, A ;
Castellví, M ;
Gelpí, J ;
Ferrer, I ;
Acarín, N ;
Pasarín, L ;
Blesa, R ;
Oliva, R .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2002, 72 (02) :266-269
[4]   Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation [J].
Raux, G ;
Gantier, R ;
Thomas-Anterion, C ;
Boulliat, J ;
Verpillat, P ;
Hannequin, D ;
Brice, A ;
Frebourg, T ;
Campion, D .
NEUROLOGY, 2000, 55 (10) :1577-1578
[5]   Presenilin 1 mutation in an African American family presenting with atypical Alzheimer dementia [J].
Rippon, GA ;
Crook, R ;
Baker, M ;
Halvorsen, E ;
Chin, S ;
Hutton, M ;
Houlden, H ;
Hardy, J ;
Lynch, T .
ARCHIVES OF NEUROLOGY, 2003, 60 (06) :884-888