| Literature DB >> 8733749 |
M Hutton1, F Busfield, M Wragg, R Crook, J Perez-Tur, R F Clark, G Prihar, C Talbot, H Phillips, K Wright, M Baker, C Lendon, K Duff, A Martinez, H Houlden, A Nichols, E Karran, G Roberts, P Roques, M Rossor, J C Venter, M D Adams, R T Cline, C A Phillips, A Goate.
Abstract
The presenilin 1 gene has recently been identified as the locus on chromosome 14 which is responsible for a large proportion of early onset, autosomal dominantly inherited Alzheimer's disease (AD). We have elucidated the intron/exon structure of the gene and designed intronic primers to enable direct sequencing of the entire coding region (10 exons) of the presenilin gene in a large number of families. This strategy has enabled us to find a further two novel mutations in the gene. We discuss the distribution of mutations and the proportions of autosomal dominant AD with a mean age of onset below 60 years caused by mutations in this gene.Entities:
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Year: 1996 PMID: 8733749 DOI: 10.1097/00001756-199602290-00029
Source DB: PubMed Journal: Neuroreport ISSN: 0959-4965 Impact factor: 1.837