The role of miR-196a in the pathogenesis of Huntington's disease
博士 === 國立成功大學 === 基礎醫學研究所 === 103 === Huntington’s disease (HD) is an inherited autosomal-dominant neurodegenerative disease that is caused by expansion of CAG repeats in the exon 1 of the huntingtin gene. The aggregation of mutant huntingtin (htt) proteins affects the central nervous system, especi...
| Main Authors: | , |
|---|---|
| Other Authors: | |
| Format: | Others |
| Language: | en_US |
| Published: |
2015
|
| Online Access: | http://ndltd.ncl.edu.tw/handle/dwmuu4 |