Загрузка...
Microglial Activation in the Pathogenesis of Huntington’s Disease
Huntington’s disease (HD) is an autosomal dominantly inherited neurodegenerative disorder caused by expanded CAG trinucleotide repeats (>36) in exon 1 of HTT gene that encodes huntingtin protein. Although HD is characterized by a predominant loss of neurons in the striatum and cortex, previous st...
Сохранить в:
| Опубликовано в: : | Front Aging Neurosci |
|---|---|
| Главные авторы: | , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Frontiers Media S.A.
2017
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5474461/ https://ncbi.nlm.nih.gov/pubmed/28674491 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnagi.2017.00193 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|