Spinocerebellar ataxia type 8：Genetic and Functional Studies of ATXN8 Gene -62 G/A Promoter SNP
碩士 === 國立臺灣師範大學 === 生命科學研究所 === 100 === Spinocerebellar ataxia type 8 (SCA8) is a hereditary neurodegenerative disorder, manifesting itself as a slowly progressive cerebellar ataxia. The penetrance of SCA8 is incomplete. SCA8 involves the expression of a CTG/CAG expansion mutation from opposite stra...
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| Format: | Others |
| Language: | zh-TW |
| Published: |
2011
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| Online Access: | http://ndltd.ncl.edu.tw/handle/88523829084666649377 |