No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.

Author:

Campion D,Brice A,Hannequin D,Charbonnier F,Dubois B,Martin C,Michon A,Penet C,Bellis M,Calenda A,Martinez M,Agid Y,Clerget-Darpoux F,Frebourg T

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference34 articles.

1. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease;Goate, A.; Chartier-Harlin, M.C.; Mullan, M.;Nature,1991

2. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease;Sherrington, R.; Rogaev, E.I.; Liang, Y.;Nature,1995

3. Mutations of the presenilin I gene in families with early-onset Alzheimer's disease;Campion, D.; Flaman, J.M.; Brice, A.;Hum Mol Genet,1995

4. Candidate gene for the chromosome 1 familial Alzheimer's disease locus;Levy-Lahad, E.; Wasco, W.; Poorkaj, P.;Science,1995

5. Apolipoprotein E: high-avidity binding to amyloid and increased frequency of type 4 allele in late onset familial Alzheimer disease;Strittmatter, W.J.; Saunders, A.M.; Schmechel, D.;Proc Natl Acad Sci USA,1993

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