Identification of a novel mutation in APP gene in a Thai subject with early-onset Alzheimer’s disease

INTRODUCTION: Early-onset Alzheimer’s disease (AD) accounts for than less 1% of all AD cases, with large variation in the reported genetic contributions of known dementia genes. Mutations in the amyloid precursor protein (APP) gene were the first to be recognized as the cause of AD. METHODS: Here, a...

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Detalles Bibliográficos
Autores principales: Van Giau, Vo, Senanarong, Vorapun, Bagyinszky, Eva, Limwongse, Chanin, An, Seong Soo A, Kim, SangYun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6231518/
https://www.ncbi.nlm.nih.gov/pubmed/30510423
http://dx.doi.org/10.2147/NDT.S180174

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6231518/
https://www.ncbi.nlm.nih.gov/pubmed/30510423
http://dx.doi.org/10.2147/NDT.S180174

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