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...

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書誌詳細
主要な著者: Zhu, Xiongwei, Babar, Asim, Siedlak, Sandra L, Yang, Qiwei, Ito, Genta, Iwatsubo, Takeshi, Smith, Mark A, Perry, George, Chen, Shu G
フォーマット: Artigo
言語:Inglês
出版事項: BioMed Central 2006
主題:
Research Article
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
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