載入...
G2019S LRRK2 mutation causing Parkinson’s disease without Lewy bodies
The G2019S leucine-rich repeat kinase 2 gene (LRRK2) mutation has been identified in a significant proportion of familial and sporadic cases of Parkinson’s disease (PD). Until now, information on the neuropathological changes associated with the G2019S LRRK2 mutation has been sparse. We report a 77-...
Na minha lista:
| Main Authors: | , , , , , |
|---|---|
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BMJ Publishing Group
2009
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3029537/ https://ncbi.nlm.nih.gov/pubmed/21686713 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr.08.2008.0632 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|