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Mutational analysis in familial Alzheimer’s disease of Han Chinese in Taiwan with a predominant mutation PSEN1 p.Met146Ile

Mutations in PSEN1, PSEN2, or APP genes are known to be causative for autosomal dominant Alzheimer’s disease (ADAD). While more than 400 mutations were reported worldwide, predominantly PSEN1, over 40 mutations have been reported in Han Chinese and were associated with earlier onset and more affecte...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Lin, Yung-Shuan, Cheng, Chih-Ya, Liao, Yi-Chu, Hong, Chen-Jee, Fuh, Jong-Ling
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7666133/
https://ncbi.nlm.nih.gov/pubmed/33188256
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-76794-9
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