Mutational analysis of the amyloid precursor protein gene in Japanese familial Alzheimer's disease kindreds

✍ Scribed by Hiroto Fujigasaki; Satoshi Naruse; Kiyotoshi Kaneko; Hideto Hirasawa; Shoji Tsuji; Tadashi Miyatake

• Publisher: Springer
• Year: 1994
• Tongue: English
• Weight: 310 KB
• Volume: 93
• Category: Article
• ISSN: 0340-6717
• DOI: 10.1007/bf00201676

✦ Synopsis

We sequenced the entire coding region of the amyloid precursor protein (APP) genes of 11 unrelated patients with Japanese familial Alzheimer's disease (FAD) in order to determine the exact frequency of known APP gene mutations and to search for novel mutations responsible for FAD. Three out of 11 (27.3%) FAD patients showed the known Val to lie mis-sense mutation at codon 717, but no other mutations were detected in the entire coding region. Analysis of exons 16 and 17 in 30 Japanese with sporadic AD revealed no mutations. Moreover, there were no significant differences in the allele frequencies of the DNA polymorphism in intron 9 among the 11 FAD, 39 sporadic AD, and 110 control subjects.