載入...
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...
Na minha lista:
| 發表在: | Front Aging Neurosci |
|---|---|
| Main Authors: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Frontiers Media S.A.
2017
|
| 主題: | |
| 在線閱讀: | 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 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|