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Measurement of LRRK2 and Ser910/935 Phosphorylated LRRK2 in Peripheral Blood Mononuclear Cells from Idiopathic Parkinson's Disease Patients

A significant number of autosomal dominantly inherited Parkinson's disease (PD) cases are due to mutations in the leucine-rich repeat kinase 2 (LRRK2) gene. In cells, these pathogenic mutations have a number of differing effects on LRRK2 enzymatic activity and protein stability. In particular, five...

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Principais autores: Nicolas Dzamko, Germaine Chua, Madelaine Ranola, Dominic B. Rowe, Glenda M. Halliday
Formato: Artigo
Idioma:Inglês
Publicado em: SAGE Publishing 2013-05-01
coleção:Journal of Parkinson’s Disease
Acesso em linha:https://doi.org/10.3233/JPD-130174
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