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Mutation screening of a haplotype block around the insulin degrading enzyme gene and association with Alzheimer's disease

✍ Scribed by Lars Feuk; Shane McCarthy; Björn Andersson; Jonathan A. Prince; Anthony J. Brookes


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
81 KB
Volume
136B
Category
Article
ISSN
1552-4841

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Mutations in the presenilin-1 (PS1) gene account for the majority of familial early-onset Alzheimer's disease (EOAD) cases. We screened the coding part of the PS1 gene for the presence of mutations in a French family with EOAD, using single strand conformation polymorphism (SSCP) analysis. Patients