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Discovery and validation of autosomal dominant Alzheimer’s disease mutations
BACKGROUND: Alzheimer’s disease (AD) is a neurodegenerative disease that is clinically characterized by progressive cognitive decline. Mutations in amyloid-β precursor protein (APP), presenilin 1 (PSEN1), and presenilin 2 (PSEN2) are the pathogenic cause of autosomal dominant AD (ADAD). However, pol...
Gorde:
| Argitaratua izan da: | Alzheimers Res Ther |
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| Egile Nagusiak: | , , , , , , , , , , , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BioMed Central
2018
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6052673/ https://ncbi.nlm.nih.gov/pubmed/30021643 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13195-018-0392-9 |
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