Phenotypical difference of Amyloid Precursor Protein (APP) V717L mutation in Japanese family
<p>Abstract</p> <p>Background</p> <p>Alzheimer’s disease (AD) is the most common form of dementia. Mutations in genes such as those encoding amyloid precursor protein (APP), presenilin 1 and presenilin 2, are responsible for early-onset familial AD.</p> <p>C...
| Main Authors: | , , , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
BMC
2012-06-01
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| Series: | BMC Neurology |
| Online Access: | http://www.biomedcentral.com/1471-2377/12/38 |