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LRRK2 function on actin and microtubule dynamics in Parkinson disease

The mutations in the LRRK2 gene cause clinically typical, late-onset Parkinson disease, strengthening the idea that the familial forms of the disease represent an important tool for the study of the idiopathic forms. Despite the great effort to describe and functionally characterize the LRRK2 gene p...

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Autores principales: Parisiadou, Loukia, Cai, Huaibin
Formato: Artigo
Lenguaje:Inglês
Publicado: Landes Bioscience 2010
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2974064/
https://ncbi.nlm.nih.gov/pubmed/21057624
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/cib.3.5.12286
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