| Literature DB >> 9225696 |
R Crook1, R Ellis, M Shanks, L J Thal, J Perez-Tur, M Baker, M Hutton, T Haltia, J Hardy, D Galasko.
Abstract
We describe a new mutation causing Alzheimer's disease (AD) in presenilin-1 (N135D) that is at the homologous site to the presenilin 2 mutation (N141I) in Volga German kindreds. The phenotype of PS1 N135D is an early-onset (34-38 years) disease. The mutation forms part of, and extends, the alpha-helical array of mutations in transmembrane 2 of the presenilins and leads to the suggestion that disruption of this helical face is the molecular insult that leads to disease.Entities:
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Year: 1997 PMID: 9225696 DOI: 10.1002/ana.410420121
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422