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Rare ABCA7 variants in 2 German families with Alzheimer disease
OBJECTIVE: The aim of this study was to identify variants associated with familial late-onset Alzheimer disease (AD) using whole-genome sequencing. METHODS: Several families with an autosomal dominant inheritance pattern of AD were analyzed by whole-genome sequencing. Variants were prioritized for r...
Tallennettuna:
| Julkaisussa: | Neurol Genet |
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| Päätekijät: | , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Wolters Kluwer
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5863691/ https://ncbi.nlm.nih.gov/pubmed/29577078 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000224 |
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