Molecular genetics of Alzheimer's disease in Italian families.

Abstract

We screened 11 families from different regions of Italy by direct sequencing of exon 17 of the APP gene. Two unrelated families carried the APP717 mutation segregating with the disease. These two families originate from two Italian regions which are considered genetically separate. Published studies have demonstrated the presence of the APP717 Val-->Ile mutation in kindreds of British or Japanese origin with early onset familial Alzheimer's disease. These data suggest that the APP717 mutation is not confined to islander families which may share common founders. From the molecular genetic point of view we also did linkage analysis. Several families, in fact, have not shown a linkage with chromosome 21 and the resolution of this dilemma required investigation of those pedigrees both with additional markers from chromosome 21 and with markers from other chromosomes.

• Authors: S Sorbi, B Nacmias, M Mortilla, P Forleo, S Piacentini, L Amaducci
• Journal: Neurochemistry international (Neurochem Int) Vol. 25 Issue 1 Pg. 81-4 (Jul 1994) ISSN: 0197-0186 [Print] England
• PMID: 7950975 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Topics

• Alzheimer Disease (genetics)
• Chromosomes, Human, Pair 14
• Exons (genetics)
• Genetic Linkage
• Humans
• Italy
• Mutation
• Pedigree