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Genetic screening in two Iranian families with early onset Alzheimer’s disease identified a novel PSEN1 mutation
A subset of early onset Alzheimer’s disease (AD) is inherited as an autosomal dominant trait and is associated with mutations in the genes encoding β-amyloid precursor protein, presenilin 1, or presenilin 2. In this study, we identified two PSEN1 mutations (one novel and one known) in two unrelated...
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| Publicado no: | Neurobiol Aging |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5743634/ https://ncbi.nlm.nih.gov/pubmed/29175279 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2017.10.011 |
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