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Cellular effects of LRRK2 mutations

Mutations in leucine-rich repeat kinase 2 (LRRK2) are a relatively common cause of inherited Parkinson's disease (PD) but the mechanism(s) by which mutations lead to disease are poorly understood. Here, I will discuss what is known about LRRK2 in cellular models, focusing on specifically on ass...

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Detalhes bibliográficos
Publicado no:Biochem Soc Trans
Autor principal: Cookson, Mark R
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4662252/
https://ncbi.nlm.nih.gov/pubmed/22988867
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BST20120165
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