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Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North Africa
Mutations in the Glucocerebrosidase gene (GBA) have recently been associated with an increased risk of Parkinson disease (PD). GBA mutations have been observed to be particularly prevalent in the Ashkenazi Jewish population. Interestingly, this population also has a high incidence of the Lrrk2 p.G20...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2970621/ https://ncbi.nlm.nih.gov/pubmed/19945510 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neulet.2009.11.066 |
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