ロード中...
LRRK2 in Parkinson's disease and dementia with Lewy bodies
BACKGROUND: Mutations in LRRK2 encoding leucine-rich repeat kinase 2 are thus far the most frequent genetic cause associated with autosomal dominant and idiopathic Parkinson's disease (PD). To examine whether LRRK2 is directly associated with neuropathology of PD and other related disorders, we...
保存先:
| 主要な著者: | , , , , , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2006
|
| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1693553/ https://ncbi.nlm.nih.gov/pubmed/17137507 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1326-1-17 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|