Over fifty missense mutations in the presenilin-1 (PSEN1) gene have been reported in families with presenile familial Alzheimer's disease (FAD). We describe a novel missense mutation (G209R) within the predicted fourth transmembrane domain of the PSEN1 in a Japanese family with presenile FAD. The af
✦ LIBER ✦
Novel APP mutation V715A associated with presenile Alzheimer’s disease in a German family
✍ Scribed by Marc Cruts; Bart Dermaut; Rosa Rademakers; Marleen Broeck; Florian Stögbauer; Christine Broeckhoven
- Publisher
- Springer
- Year
- 2003
- Tongue
- English
- Weight
- 185 KB
- Volume
- 250
- Category
- Article
- ISSN
- 0340-5354
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