Glucocerebrosidase mutations in a Serbian Parkinson's disease population
✍ Scribed by K. R. Kumar; A. Ramirez; A. Göbel; N. Kresojević; M. Svetel; K. Lohmann; C. M Sue; A. Rolfs; J. R. Mazzulli; R. N. Alcalay; D. Krainc; C. Klein; V. Kostic; A. Grünewald
- Book ID
- 115236485
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- English
- Weight
- 454 KB
- Volume
- 20
- Category
- Article
- ISSN
- 1351-5101
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
FIG. 1. MRI showed symmetric (A) hypointensity signal on T1weighted imaging and (B) hyperintensity signal on T2-weighted imaging in bilateral substantia nigra on admission. A repeated MRI after 3 months showed resolution of the lesions on (C) T2-weighted imaging and (D) T1-weighted imaging.
## Abstract An association between mutations in the __glucocerebrosidase__ (__GBA__) gene and Parkinson's disease (PD) has been reported in several populations. We searched for four common __GBA__ mutations (L444P, F213I, R353W, and N370S) in 402 Chinese PD patients and 413 age‐ and sex‐matched con
## Abstract Recent studies have reported an association between the glucocerebrosidase (__GBA__) gene and Parkinson's disease (PD). To elucidate the role of this gene in our population, we screened 395 PD patients and 483 controls from southern Italy for the N370S and the L444P mutations. We found