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...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Zhu, Xiongwei, Babar, Asim, Siedlak, Sandra L, Yang, Qiwei, Ito, Genta, Iwatsubo, Takeshi, Smith, Mark A, Perry, George, Chen, Shu G
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2006
Fag:
Research Article
Online adgang: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
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker