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Lrrk2 mutations in South America: A study of Chilean Parkinson's disease

Pathogenic substitutions in the leucine-rich repeat kinase 2 protein (Lrrk2), R1441G and G2019S, are a prevalent cause of autosomal dominant and sporadic Parkinson's disease in the Northern Spanish population. In this study we examined the frequency of these two substitutions in 166 Parkinson&#...

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Detalhes bibliográficos
Main Authors: Perez-Pastene, Carolina, Cobb, Stephanie A., Díaz-Grez, Fernando, Hulihan, Mary M., Miranda, Marcelo, Venegas, Pablo, Godoy, Osvaldo Trujillo, Kachergus, Jennifer M., Ross, Owen A., Layson, Luis, Farrer, Matthew J., Segura-Aguilar, Juan
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1986707/
https://ncbi.nlm.nih.gov/pubmed/17614198
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neulet.2007.06.021
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