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APP, PSEN1, and PSEN2 Mutations in Asian Patients with Early-Onset Alzheimer Disease
The number of patients with Alzheimer’s disease (AD) is rapidly increasing in Asia. Mutations in the amyloid protein precursor (APP), presenilin-1 (PSEN1), and presenilin-2 (PSEN2) genes can cause autosomal dominant forms of early-onset AD (EOAD). Although these genes have been extensively studied,...
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| Publicado en: | Int J Mol Sci |
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| Autores principales: | , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
MDPI
2019
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6801447/ https://ncbi.nlm.nih.gov/pubmed/31557888 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms20194757 |
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