论文信息 - Screening for the β-amyloid precursor protein mutation (APP717: Val → Ile) in extended pedigrees with early onset Alzheimer's disease - 字舞流文

Screening for the β-amyloid precursor protein mutation (APP717: Val → Ile) in extended pedigrees with early onset Alzheimer's disease

J. Hardy | C. Broeckhoven | A. Goate | K. Hamandi | H. Backhovens | Jean-Jacques Martin | M. Mullan | F. Crawford | M. Chartier-Harlin | J. Hardy

[1] E M Wijsman,et al. Linkage analysis of familial Alzheimer disease, using chromosome 21 markers. , 1991, American journal of human genetics.

[2] M. Pericak-Vance,et al. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease , 1991, Nature.

[3] Y. Sakaki,et al. Genomic organization of the human-amyloid beta-protein precursor gene. , 1990, Gene.

[4] I. Rainero,et al. Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder , 1990, Nature.

[5] Martin Farrall,et al. PREDISPOSING LOCUS FOR ALZHEIMER'S DISEASE ON CHROMOSOME 21 , 1989, The Lancet.

[6] S. M. Sumi,et al. Absence of linkage of chromosome 21q21 markers to familial Alzheimer's disease. , 1988, Science.

[7] J. Haines,et al. The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid β-protein gene , 1987, Nature.

[8] C. Broeckhoven,et al. Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families , 1987, Nature.

[9] D. Pollen,et al. The genetic defect causing familial Alzheimer's disease maps on chromosome 21. , 1987, Science.