Загрузка...
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...
Сохранить в:
| Опубликовано в: : | Neurobiol Aging |
|---|---|
| Главные авторы: | , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2017
|
| Предметы: | |
| Online-ссылка: | 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 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|