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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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Main Authors: | , , , , , , , , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
2007
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Assuntos: | |
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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