SCREENING FOR THE BETA-AMYLOID PRECURSOR PROTEIN MUTATION (APP717-VAL-]ILE) IN EXTENDED PEDIGREES WITH EARLY ONSET ALZHEIMERS-DISEASE

被引:58
作者
CHARTIERHARLIN, MC
CRAWFORD, F
HAMANDI, K
MULLAN, M
GOATE, A
HARDY, J
BACKHOVENS, H
MARTIN, JJ
VAN BROECKHOVEN, C
机构
[1] ST MARYS HOSP, SCH MED, DEPT BIOCHEM, ALZHEIMERS DIS RES GRP, LONDON W2 1PG, ENGLAND
[2] ST MARYS HOSP, SCH MED, DEPT NEUROL, LONDON W2 1PG, ENGLAND
[3] UNIV INSTELLING ANTWERP, BORN BUNGE FDN, NEUROGENET LAB, B-2610 WILRIJK, BELGIUM
[4] UNIV INSTELLING ANTWERP, BORN BUNGE FDN, NEUROPATHOL LAB, B-2610 WILRIJK, BELGIUM
关键词
ALZHEIMERS DISEASE; CHROMOSOME-21; BETA-AMYLOID PRECURSOR PROTEIN (APP);
D O I
10.1016/0304-3940(91)90738-F
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Screening for the APP717 mutation in 5 further families with early onset Alzheimer's disease failed to reveal further cases with this variant. Screening a further 100 normal individuals for this mutation also failed to reveal further occurrences of this variant in the general population. Sequencing of exons 16 and 17 of the beta-amyloid precursor protein gene (the exons which encode the beta-amyloid fragment) in pedigree FAD4 revealed them to be of normal sequence. The significance of these observations to the genetics of Alzheimer's disease is discussed.
引用
收藏
页码:134 / 135
页数:2
相关论文
共 9 条
  • [1] SEGREGATION OF A MISSENSE MUTATION IN THE AMYLOID PRECURSOR PROTEIN GENE WITH FAMILIAL ALZHEIMERS-DISEASE
    GOATE, A
    CHARTIERHARLIN, MC
    MULLAN, M
    BROWN, J
    CRAWFORD, F
    FIDANI, L
    GIUFFRA, L
    HAYNES, A
    IRVING, N
    JAMES, L
    MANT, R
    NEWTON, P
    ROOKE, K
    ROQUES, P
    TALBOT, C
    PERICAKVANCE, M
    ROSES, A
    WILLIAMSON, R
    ROSSOR, M
    OWEN, M
    HARDY, J
    [J]. NATURE, 1991, 349 (6311) : 704 - 706
  • [2] GOATE AM, 1989, LANCET, V1, P352
  • [3] ABSENCE OF LINKAGE OF CHROMOSOME 21Q21 MARKERS TO FAMILIAL ALZHEIMERS-DISEASE
    SCHELLENBERG, GD
    BIRD, TD
    WIJSMAN, EM
    MOORE, DK
    BOEHNKE, M
    BRYANT, EM
    LAMPE, TH
    NOCHLIN, D
    SUMI, SM
    DEEB, SS
    BEYREUTHER, K
    MARTIN, GM
    [J]. SCIENCE, 1988, 241 (4872) : 1507 - 1510
  • [4] SCHELLENBERG GD, 1991, AM J HUM GENET, V48, P563
  • [5] THE GENETIC-DEFECT CAUSING FAMILIAL ALZHEIMERS-DISEASE MAPS ON CHROMOSOME-21
    STGEORGEHYSLOP, PH
    TANZI, RE
    POLINSKY, RJ
    HAINES, JL
    NEE, L
    WATKINS, PC
    MYERS, RH
    FELDMAN, RG
    POLLEN, D
    DRACHMAN, D
    GROWDON, J
    BRUNI, A
    FONCIN, JF
    SALMON, D
    FROMMELT, P
    AMADUCCI, L
    SORBI, S
    PIACENTINI, S
    STEWART, GD
    HOBBS, WJ
    CONNEALLY, PM
    GUSELLA, JF
    [J]. SCIENCE, 1987, 235 (4791) : 885 - 890
  • [6] GENETIC-LINKAGE STUDIES SUGGEST THAT ALZHEIMERS-DISEASE IS NOT A SINGLE HOMOGENEOUS DISORDER
    STGEORGEHYSLOP, PH
    HAINES, JL
    FARRER, LA
    POLINSKY, R
    VAN BROECKHOVEN, C
    GOATE, A
    MCLACHLAN, DRC
    ORR, H
    BRUNI, AC
    SORBI, S
    RAINERO, I
    FONCIN, JF
    POLLEN, D
    CANTU, JM
    TUPLER, R
    VOSKRESENSKAYA, N
    MAYEUX, R
    GROWDON, J
    FRIED, VA
    MYERS, RH
    NEE, L
    BACKHOVENS, H
    MARTIN, JJ
    ROSSOR, M
    OWEN, MJ
    MULLAN, M
    PERCY, ME
    KARLINSKY, H
    RICH, S
    HESTON, L
    MONTESI, M
    MORTILLA, M
    NACMIAS, N
    GUSELLA, JF
    HARDY, JA
    [J]. NATURE, 1990, 347 (6289) : 194 - 197
  • [7] THE GENETIC-DEFECT IN FAMILIAL ALZHEIMERS-DISEASE IS NOT TIGHTLY LINKED TO THE AMYLOID BETA-PROTEIN GENE
    TANZI, RE
    STGEORGEHYSLOP, PH
    HAINES, JL
    POLINSKY, RJ
    NEE, L
    FONCIN, JF
    NEVE, RL
    MCCLATCHEY, AI
    CONNEALLY, PM
    GUSELLA, JF
    [J]. NATURE, 1987, 329 (6135) : 156 - 157
  • [8] VAN BROECKHOVEN C, 1987, NATURE, V329, P153
  • [9] GENOMIC ORGANIZATION OF THE HUMAN AMYLOID BETA-PROTEIN PRECURSOR GENE
    YOSHIKAI, S
    SASAKI, H
    DOHURA, K
    FURUYA, H
    SAKAKI, Y
    [J]. GENE, 1990, 87 (02) : 257 - 263