Gene mutations associated with early onset familial Alzheimer’s disease in China: An overview and current status

BACKGROUND: Mutations of three causative genes, namely presenilin 1 (PSEN1), presenilin 2 (PSEN2), and amyloid precursor protein (APP), have been identified as the major causes of early‐onset familial Alzheimer's disease (EOFAD). The prevalence of causative gene mutations in patients with EOFAD...

Descripción completa

Detalles Bibliográficos
Autores principales: Qin, Qi, Yin, Yunsi, Wang, Yan, Lu, Yuanyuan, Tang, Yi, Jia, Jianping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7549583/
https://www.ncbi.nlm.nih.gov/pubmed/32767553
http://dx.doi.org/10.1002/mgg3.1443

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7549583/
https://www.ncbi.nlm.nih.gov/pubmed/32767553
http://dx.doi.org/10.1002/mgg3.1443

Ejemplares similares