Familial Alzheimer's disease: Site of mutation influences clinical phenotype
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D. Pollen | P. S. St George-Hyslop | D. Drachman | B. Ghetti | C. Lippa | J. Swearer | D. Nochlin | L. Nee | K. Kane | T. Bird
[1] C. Lippa,et al. Familial Alzheimer's disease: genetic influences on the disease process (Review). , 1999, International journal of molecular medicine.
[2] J. Wegiel,et al. Cell-Type-Specific Enhancement of Amyloid-β Deposition in a Novel Presenilin-1 Mutation (P117L) , 1998, Journal of neuropathology and experimental neurology.
[3] John Q. Trojanowski,et al. Consensus Recommendations for the Postmortem Diagnosis of Alzheimer’s Disease , 1997, Neurobiology of Aging.
[4] J. Rommens,et al. Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene , 1995, Nature.
[5] E M Wijsman,et al. A familial Alzheimer's disease locus on chromosome 1 , 1995, Science.
[6] S. Sorbi,et al. Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's disease , 1995, Annals of neurology.
[7] M. Rossor,et al. Age of onset in familial early onset Alzheimer's disease correlates with genetic aetiology. , 1993, American journal of medical genetics.
[8] J. Haines,et al. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. , 1993, Science.
[9] D. Pollen,et al. Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14 , 1992, Nature Genetics.
[10] M. Pericak-Vance,et al. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease , 1991, Nature.
[11] M. Folstein,et al. Clinical diagnosis of Alzheimer's disease , 1984, Neurology.