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Association between Parkinson's disease and G2019S and R1441C mutations of the LRRK2 gene
In recent genome-wide association studies (GWAS), 11 risk loci were identified in patients with familial and sporadic Parkinson's disease (PD) in different populations. The LRRK2 gene was found to be a mutation hot spot in European and Asian populations. The aim of the present study was to inve...
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| Publicat a: | Exp Ther Med |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
D.A. Spandidos
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4578097/ https://ncbi.nlm.nih.gov/pubmed/26622505 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2015.2659 |
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