Загрузка...
Early Onset Alzheimer’s Disease with Spastic Paraparesis, Dysarthria and Seizures and N135S Mutation in PSEN1
OBJECTIVE: Early onset familial Alzheimer’s disease (EOFAD) can be caused by mutations in genes for amyloid precursor protein (APP), presenilin 1 (PSEN1) or presenilin 2 (PSEN2). There is considerable phenotypic variability in EOFAD, including some patients with spastic paraparesis. The objective is...
Сохранить в:
| Главные авторы: | , , , , , , |
|---|---|
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2008
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2750842/ https://ncbi.nlm.nih.gov/pubmed/18580586 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/WAD.0b013e3181732399 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|