Characterization of the Spinocerebellar Ataxia Type 22 Gene
碩士 === 國立陽明大學 === 生命科學暨基因體科學研究所 === 96 === Spinocerebellar ataxias (SCAs) are a group of hereditary neurodegenerative disorders characterized by loss coordination of voluntary muscular movement due to dysfunction of the cerebellum and its afferent and efferent connections. This group of diseases is...
Main Authors: | , |
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Other Authors: | |
Format: | Others |
Language: | en_US |
Published: |
2008
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Online Access: | http://ndltd.ncl.edu.tw/handle/99363389985998450107 |