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Behavioral, neurochemical, and pathological alterations in BAC transgenic G2019S LRRK2 rats

Mutations in leucine-rich repeated kinase 2 (LRRK2) cause autosomal dominant late-onset Parkinson’s disease (PD), and the G2019S mutation in the kinase domain of LRRK2 is the most common genetic cause of familial PD. Enhanced kinase activity of G2019S LRRK2 is a suspected mechanism for carriers to d...

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Detalhes bibliográficos
Publicado no:Neurobiol Aging
Main Authors: Lee, Jang-Won, Tapias, Victor, Di Maio, Roberto, Greenamyre, J. Timothy, Cannon, Jason R.
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5289148/
https://ncbi.nlm.nih.gov/pubmed/25174649
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2014.07.011
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