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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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Detalles Bibliográficos
Autores principales:	Park, Hyun-Kyung, Na, Duk Lyul, Lee, Jae-Hong, Kim, Jong-Won, Ki, Chang-Seok
Formato:	Texto
Lenguaje:	English
Publicado:	The Korean Academy of Medical Sciences 2008
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2526428/ https://www.ncbi.nlm.nih.gov/pubmed/18437002 http://dx.doi.org/10.3346/jkms.2008.23.2.213

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