Molecular Genetic and Functional Studies of Leucine-Rich Repeat Kinase 2 (LRRK2) Gene Variations in Taiwanese Parkinson's Disease
碩士 === 國立臺灣師範大學 === 生命科學研究所 === 100 === Mutations in leucine-rich repeat kinase 2 (LRRK2, encoding dardarin) is the most common cause of autosomal dominant PD. LRRK2 protein is expressed ubiquitously, particularly in the central nervous system, major organs and also in the lymphocytes. Previously...
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| Format: | Others |
| Language: | zh-TW |
| Published: |
2011
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| Online Access: | http://ndltd.ncl.edu.tw/handle/05937545892631976406 |