Загрузка...
Frontotemporal Dementia Caused by CHMP2B Mutations
CHMP2B mutations are a rare cause of autosomal dominant frontotemporal dementia (FTD). The best studied example is frontotemporal dementia linked to chromosome 3 (FTD-3) which occurs in a large Danish family, with a further CHMP2B mutation identified in an unrelated Belgian familial FTD patient. The...
Сохранить в:
| Главные авторы: | , , , , |
|---|---|
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Bentham Science Publishers Ltd
2011
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3182073/ https://ncbi.nlm.nih.gov/pubmed/21222599 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/156720511795563764 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|