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ERKed by LRRK2: A cell biological perspective on hereditary and sporadic Parkinson’s disease

The leucine rich repeat kinase 2 (LRRK2/dardarin) is implicated in autosomal dominant familial and sporadic Parkinson’s disease (PD); mutations in LRRK2 account for up to 40% of PD cases in some populations. LRRK2 is a large protein with a kinase domain, a GTPase domain, and multiple potential prote...

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Autors principals: Verma, Manish, Steer, Erin K., Chu, Charleen T.
Format: Artigo
Idioma:Inglês
Publicat: 2013
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4016799/
https://ncbi.nlm.nih.gov/pubmed/24225420
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbadis.2013.11.005
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