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Identification of PSEN1 and APP Gene Mutations in Korean Patients with Early-Onset Alzheimer's Disease

Although mutations in three genes, amyloid precursor protein (APP), presenilin 1 (PSEN1), and presenilin 2 (PSEN2), have been identified as genetic causes of early-onset Alzheimer's disease (EOAD), there has been a single report on a PSEN1 mutation in Koreans. In the present study, we performed...

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Bibliografiske detaljer
Main Authors: Park, Hyun-Kyung, Na, Duk Lyul, Lee, Jae-Hong, Kim, Jong-Won, Ki, Chang-Seok
Format: Artigo
Sprog:Inglês
Udgivet: The Korean Academy of Medical Sciences 2008
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2526428/
https://ncbi.nlm.nih.gov/pubmed/18437002
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3346/jkms.2008.23.2.213
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