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G2019S LRRK2 mutation causing Parkinson’s disease without Lewy bodies

The G2019S leucine-rich repeat kinase 2 gene (LRRK2) mutation has been identified in a significant proportion of familial and sporadic cases of Parkinson’s disease (PD). Until now, information on the neuropathological changes associated with the G2019S LRRK2 mutation has been sparse. We report a 77-...

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Detalhes bibliográficos
Main Authors: Gaig, Carles, Martí, María José, Ezquerra, Mario, Cardozo, Adriana, Rey, Maria Jesus, Tolosa, Eduardo
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Publishing Group 2009
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3029537/
https://ncbi.nlm.nih.gov/pubmed/21686713
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr.08.2008.0632
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