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. 2002 Feb;72(2):266–269. doi: 10.1136/jnnp.72.2.266
A novel mutation (V89L) in the presenilin 1 gene in a family with early onset Alzheimer's disease and marked behavioural disturbances
R Queralt
1, M Ezquerra
1, A Lleo
1, M Castellvi
1, J Gelpi
1, I Ferrer
1, N Acarin
1, L Pasarin
1, R Blesa
1, R Oliva
1
R Queralt
1Genetics Service, Hospital Clínic, Universitat de Barcelona, Spain. roliva@clinic.ub.es
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M Ezquerra
1Genetics Service, Hospital Clínic, Universitat de Barcelona, Spain. roliva@clinic.ub.es
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A Lleo
1Genetics Service, Hospital Clínic, Universitat de Barcelona, Spain. roliva@clinic.ub.es
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M Castellvi
1Genetics Service, Hospital Clínic, Universitat de Barcelona, Spain. roliva@clinic.ub.es
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J Gelpi
1Genetics Service, Hospital Clínic, Universitat de Barcelona, Spain. roliva@clinic.ub.es
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I Ferrer
1Genetics Service, Hospital Clínic, Universitat de Barcelona, Spain. roliva@clinic.ub.es
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N Acarin
1Genetics Service, Hospital Clínic, Universitat de Barcelona, Spain. roliva@clinic.ub.es
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L Pasarin
1Genetics Service, Hospital Clínic, Universitat de Barcelona, Spain. roliva@clinic.ub.es
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R Blesa
1Genetics Service, Hospital Clínic, Universitat de Barcelona, Spain. roliva@clinic.ub.es
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R Oliva
1Genetics Service, Hospital Clínic, Universitat de Barcelona, Spain. roliva@clinic.ub.es
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1Genetics Service, Hospital Clínic, Universitat de Barcelona, Spain. roliva@clinic.ub.es
PMCID: PMC1737723 PMID: 11796781