Mutation analysis of the presenilin-1 and -2 genes in a population based sample of early-onset Alzheimer's disease.

被引：0
|
作者：
Cruts, M
Backhovens, H
Van den Broeck, M
Serneels, S
Sherrington, R
Hutton, M
Hofman, A
St Georges-Hyslop, PH
Hardy, J
van Duijn, CM
Van Broeckhoven, C
机构：
[1] Univ Antwerp VIB, Dept Biochem,Bom Bunge Fdn, BBS, Neurogenet Lab, B-2020 Antwerp, Belgium
[2] Univ Toronto, Dept Med & Biophys, Ctr Res Neurodegenerat Dis, Toronto, ON, Canada
[3] Mayo Clin Jacksonville, Jacksonville, AL USA
[4] Erasmus Univ, Dept Epidemiol & Biostat, NL-3000 DR Rotterdam, Netherlands
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1997年 / 61卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
1931
引用
收藏
页码：A330 / A330
页数：1
相关论文
共 50 条
  • [1] Splicing mutation of Presenilin-1 gene for early-onset familial Alzheimer's disease
    Sato, S
    Kamino, K
    Miki, T
    Doi, A
    Ii, K
    St George-Hyslop, PH
    Ogihara, T
    Sakaki, Y
    HUMAN MUTATION, 1998, : S91 - S94
  • [2] Genetic association of the presenilin-1 regulatory region with early-onset Alzheimer's disease in a population-based sample
    Cornelia M van Duijn
    Marc Cruts
    Jessie Theuns
    Geert Van Gassen
    Hubert Backhovens
    Marleen van den Broeck
    Anita Wehnert
    Sally Serneels
    Albert Hofman
    Christine Van Broeckhoven
    European Journal of Human Genetics, 1999, 7 : 801 - 806
  • [3] Genetic association of the presenilin-1 regulatory region with early-onset Alzheimer's disease in a population-based sample
    van Duijn, CM
    Cruts, M
    Theuns, J
    Van Gassen, G
    Backhovens, H
    van den Broeck, M
    Wehnert, A
    Serneels, S
    Hofman, A
    Van Broeckhoven, C
    EUROPEAN JOURNAL OF HUMAN GENETICS, 1999, 7 (07) : 801 - 806
  • [4] Early-onset Alzheimer's disease with a presenilin-1 mutation at the site corresponding to the Volga German presenilin-2 mutation
    Crook, R
    Ellis, R
    Shanks, M
    Thal, LJ
    PerezTur, J
    Baker, M
    Hutton, M
    Haltia, T
    Hardy, J
    Galasko, D
    ANNALS OF NEUROLOGY, 1997, 42 (01) : 124 - 128
  • [5] Corticobasal Syndrome in a Family with Early-Onset Alzheimer's Disease Linked to a Presenilin-1 Gene Mutation
    Navarro, Eloisa
    De Andres, Clara
    Guerrero, Carmen
    Gimenez-Roldan, Santiago
    MOVEMENT DISORDERS CLINICAL PRACTICE, 2015, 2 (04): : 388 - 394
  • [6] Early-onset Alzheimer's disease caused by a novel mutation at codon 219 of the presenilin-1 gene
    Smith, MJ
    Gardner, RJM
    Knight, MA
    Forrest, SM
    Beyreuther, K
    Storey, E
    McLean, CA
    Cotton, RGH
    Cappal, R
    Masters, CL
    NEUROREPORT, 1999, 10 (03) : 503 - 507
  • [7] Point mutation in exon 4 of presenilin-1 gene and early-onset familial Alzheimer disease
    Yu Liao
    Neural Regeneration Research, 2006, (06) : 493 - 496
  • [8] The genotype 2/2 of the presenilin-1 polymorphism is decreased in Spanish early-onset Alzheimer's disease
    Ezquerra, M
    Blesa, R
    Tolosa, E
    Pousa, SL
    Aguilar, M
    Pena, J
    Van Broeckhoven, C
    Ballesta, F
    Oliva, R
    NEUROSCIENCE LETTERS, 1997, 227 (03) : 201 - 204
  • [9] Posterior Accumulation of Tau and Concordant Hypometabolism in an Early-Onset Alzheimer's Disease Patient with Presenilin-1 Mutation
    Smith, Ruben
    Wibom, Moa
    Olsson, Tomas
    Hagerstrom, Douglas
    Jogi, Jonas
    Rabinovici, Gil D.
    Hansson, Oskar
    JOURNAL OF ALZHEIMERS DISEASE, 2016, 51 (02) : 339 - 343
  • [10] The development of Presenilin-1 (PS-1) as a clinical diagnostic test for early-onset familial Alzheimer's disease.
    Ananth, UA
    Jones, JG
    Fafel, KC
    Seltzer, WK
    St George-Hyslop, PH
    Boss, MA
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A217 - A217
12345