Leucine-Rich Repeat Kinase 2-Linked Parkinson’s Disease: Clinical and Molecular Findings
Mutations in Leucine-rich repeat kinase 2 (LRRK2) gene are the most common cause of sporadic and familial late onset Parkinson’s disease (PD). The G2019S common mutation has been identified about 1% of sporadic cases and 4–7% of familial cases. Over 50 variants have since been identified in LRRK2, a...
| المؤلفون الرئيسيون: | , |
|---|---|
| التنسيق: | مقال |
| اللغة: | English |
| منشور في: |
Korean Movement Disorder Society
2010-10-01
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| سلاسل: | Journal of Movement Disorders |
| الموضوعات: | |
| الوصول للمادة أونلاين: | http://e-jmd.org/upload/jmd-3-2-25-1.pdf |