遗传学
生物
基因座(遗传学)
阿尔茨海默病
错义突变
等位基因
基因
遗传连锁
突变
位置克隆
疾病
医学
病理
作者
Robin Sherrington,Е. И. Рогаев,Yuh‐Jin Liang,Ekaterina Rogaeva,Georges Lévesque,Masaki Ikeda,Hongbo Chi,Chiao‐Feng Lin,Li Guo,K. Holman,T. Tsuda,Lynn Mar,J F Foncin,Amalia C. Bruni,M. P. Montesi,Sandro Sorbi,Innocenzo Rainero,Lorenzo Pinessi,Linda E. Nee,Ilya Chumakov
出处
期刊:Nature
[Springer Nature]
日期:1995-06-01
卷期号:375 (6534): 754-760
被引量:4021
摘要
Some cases of Alzheimer's disease are inherited as an autosomal dominant trait. Genetic linkage studies have mapped a locus (AD3) associated with susceptibility to a very aggressive form of Alzheimer's disease to chromosome 14q24.3. We have defined a minimal cosegregating region containing the AD3 gene, and isolated at least 19 different transcripts encoded within this region. One of these transcripts (S182) corresponds to a novel gene whose product is predicted to contain multiple transmembrane domains and resembles an integral membrane protein. Five different missense mutations have been found that cosegregate with early-onset familial Alzheimer's disease. Because these changes occurred in conserved domains of this gene, and are not present in normal controls, they are likely to be causative of AD3.
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