Using animal model to study the regulatory role of Supt4h in Huntington’s disease
碩士 === 國立陽明大學 === 生化暨分子生物研究所 === 100 === Huntington’s disease (HD), an inherited neurodegenerative disorder, is caused by expanded CAG repeats in the exon 1 of huntingtin gene, and primarily affects the striatum and cortex in the brain. Several studies have indicated that polyQ aggregation of mutant...
| Main Authors: | , |
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| Other Authors: | |
| Format: | Others |
| Language: | en_US |
| Published: |
2012
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| Online Access: | http://ndltd.ncl.edu.tw/handle/32355977308016679173 |