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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Autors principals: Zhu, Xiongwei, Babar, Asim, Siedlak, Sandra L, Yang, Qiwei, Ito, Genta, Iwatsubo, Takeshi, Smith, Mark A, Perry, George, Chen, Shu G
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2006
Matèries:
Research Article
Accés en línia: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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