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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...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Nishioka, Kenya, Vilariño-Güell, Carles, Cobb, Stephanie A., Kachergus, Jennifer M., Ross, Owen A., Wider, Christian, Gibson, Rachel A., Hentati, Faycal, Farrer, Matthew J.
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: 2009
Θέματα:
Διαθέσιμο Online: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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