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: Nishioka, Kenya, Vilariño-Güell, Carles, Cobb, Stephanie A., Kachergus, Jennifer M., Ross, Owen A., Wider, Christian, Gibson, Rachel A., Hentati, Faycal, Farrer, Matthew J.
格式: Artigo
語言:Inglês
出版: 2009
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Article
在線閱讀: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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