ロード中...
Genomewide linkage study of modifiers of LRRK2-related Parkinson’s disease
BACKGROUND: Mutations in the leucine-rich repeat kinase 2 gene (LRRK2), located at 12q12, are the most common known genetic causes of Parkinson’s disease (PD). Studies of LRRK2 mutation carriers have shown incomplete and age-dependent penetrance and previous studies have suggested that inherited sus...
保存先:
主要な著者: | , , , , , , , , , |
---|---|
フォーマット: | Artigo |
言語: | Inglês |
出版事項: |
2011
|
主題: | |
オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3346677/ https://ncbi.nlm.nih.gov/pubmed/21661047 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.23781 |
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!
|