Three different mutations of presenilin 1 gene in early-onset Alzheimer's disease families

被引:60
作者
Kamino, K
Sato, S
Sakaki, Y
Yoshiiwa, A
Nishiwaki, Y
Takeda, M
Tanabe, H
Nishimura, T
Ii, K
StGeorgeHyslop, PH
Miki, T
Ogihara, T
机构
[1] UNIV TOKYO,INST MED SCI,CTR HUMAN GENOME,TOKYO,JAPAN
[2] OSAKA UNIV,SCH MED,DEPT NEUROPSYCHIAT,OSAKA,JAPAN
[3] UNIV TOKUSHIMA,SCH MED,DEPT PATHOL 1,TOKUSHIMA 770,JAPAN
[4] TORONTO HOSP,DEPT MED,CTR RES NEURODEGENERAT DIS,TORONTO,ON M5T 2S8,CANADA
[5] TORONTO HOSP,DEPT NEUROL,CTR RES NEURODEGENERAT DIS,TORONTO,ON M5T 2S8,CANADA
[6] UNIV TORONTO,DEPT MED BIOPHYS,TORONTO,ON,CANADA
关键词
Alzheimer's disease; Presenilin; 1; Missense mutation; transmembrane domain; dominant inheritance; penetrance;
D O I
10.1016/0304-3940(96)12587-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Presenilin-1 (PS-1) gene of three Japanese pedigrees with early-onset familial Alzheimer's disease (FAD) disclosed two novel missense mutations resulting in Val96Phe and Ile213Thr, and one mutation resulting in His163Arg, The mean age at onset in a family with His163Arg mutation was similar to those reported in other families with His163Arg. Our results suggested the existence of a variety of PS-1 mutations, and that early-onset FAD with PS-1 mutations is highly penetrant and is only rarely subject to modulation by generic or environmental modifying factors.
引用
收藏
页码:195 / 198
页数:4
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