LRRK2 in Transcription and Translation Regulation: Relevance for Parkinson’s Disease

Parkinson’s disease (PD) is the most common neurodegenerative movement disorder and is characterized by the selective loss of dopaminergic neurons and the presence of Lewy bodies. Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are the most frequent cause of both familial and sporadic PD....

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Detalles Bibliográficos
Autores principales: Dorval, Véronique, Hébert, Sébastien S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276974/
https://www.ncbi.nlm.nih.gov/pubmed/22363314
http://dx.doi.org/10.3389/fneur.2012.00012

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276974/
https://www.ncbi.nlm.nih.gov/pubmed/22363314
http://dx.doi.org/10.3389/fneur.2012.00012

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