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A rare missense variant in CASP7 is associated with familial late-onset Alzheimer disease
INTRODUCTION: The genetic architecture of Alzheimer disease (AD) is only partially understood. METHODS: We conducted an association study for AD using whole sequence data from 507 genetically enriched AD cases (i.e., cases having close relatives affected by AD) and 4,917 cognitively healthy controls...
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| Veröffentlicht in: | Alzheimers Dement |
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| Hauptverfasser: | , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2019
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6408965/ https://ncbi.nlm.nih.gov/pubmed/30503768 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jalz.2018.10.005 |
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