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LRRK2 gene G2019S mutation and SNPs [haplotypes] in subtypes of Parkinson’s disease
Mutation within the Leucine-rich repeat kinase 2 (LRRK2) gene has been identified as a cause of autosomal dominant Parkinson’s disease (PD). The purpose of this study was to determine the frequency of G2019S mutation and whether the differences in the allele and genotype distribution of six SNPs wit...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2761091/ https://ncbi.nlm.nih.gov/pubmed/18752982 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.parkreldis.2008.05.004 |
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