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Pathological Functions of LRRK2 in Parkinson’s Disease

Mutations in the gene encoding leucine-rich repeat kinase 2 (LRRK2) are common genetic risk factors for both familial and sporadic Parkinson’s disease (PD). Pathogenic mutations in LRRK2 have been shown to induce changes in its activity, and abnormal increase in LRRK2 kinase activity is thought to c...

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Publicado en:Cells
Autores principales: Jeong, Ga Ram, Lee, Byoung Dae
Formato: Artigo
Lenguaje:Inglês
Publicado: MDPI 2020
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC7759975/
https://ncbi.nlm.nih.gov/pubmed/33266247
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells9122565
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