LRRK2 mutant knock-in mouse models: therapeutic relevance in Parkinson's disease

Mutations in the leucine-rich repeat kinase 2 gene (LRRK2) are one of the most frequent genetic causes of both familial and sporadic Parkinson’s disease (PD). Mounting evidence has demonstrated pathological similarities between LRRK2-associated PD (LRRK2-PD) and sporadic PD, suggesting that LRRK2 is...

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Detalles Bibliográficos
Autores principales: Chang, Eunice Eun Seo, Ho, Philip Wing-Lok, Liu, Hui-Fang, Pang, Shirley Yin-Yu, Leung, Chi-Ting, Malki, Yasine, Choi, Zoe Yuen-Kiu, Ramsden, David Boyer, Ho, Shu-Leong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842874/
https://www.ncbi.nlm.nih.gov/pubmed/35152914
http://dx.doi.org/10.1186/s40035-022-00285-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842874/
https://www.ncbi.nlm.nih.gov/pubmed/35152914
http://dx.doi.org/10.1186/s40035-022-00285-2

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