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...

Descripción completa

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

Internet

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

Ejemplares similares