Molecular Characterization of LRRK2 Variations in Taiwanese Parkinson’s Disease
碩士 === 國立臺灣師範大學 === 生命科學研究所 === 99 === Mutations in PARK8 associated leucine-rich repeat kinase 2 (LRRK2) have been shown to be the leading cause of autosomal dominant Parkinson's disease (PD). The multidomain LRRK2 is expressed ubiquitously, including the central nervous system and various org...
| Main Authors: | , |
|---|---|
| Other Authors: | |
| Format: | Others |
| Language: | zh-TW |
| Published: |
2010
|
| Online Access: | http://ndltd.ncl.edu.tw/handle/66068979150969846216 |