Glucocerebrosidasemutations in a Serbian Parkinson's disease population-Reference-Cited by-同舟云学术

Glucocerebrosidasemutations in a Serbian Parkinson's disease population

Published:2012-07-20 Issue:2 Volume:20 Page:402-405
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Kumar K. R.,Ramirez A.,Göbel A.¹,Kresojević N.²,Svetel M.²,Lohmann K.¹,M Sue C.³,Rolfs A.⁴,Mazzulli J. R.⁵,Alcalay R. N.⁶,Krainc D.⁵,Klein C.¹,Kostic V.²,Grünewald A.¹

Affiliation:

1. Department of Neurology; Section of Clinical and Molecular Neurogenetics; University of Lübeck; Lübeck; Germany

2. Institute of Neurology CCS; School of Medicine; University of Belgrade; Belgrade; Serbia

3. Department of Neurogenetics; Kolling Institute of Medical Research; Royal North Shore Hospital, and University of Sydney; Sydney; NSW; Australia

4. Albrecht-Kossel-Institute for Neuroregeneration; University of Rostock; Rostock; Germany

5. Department of Neurology; Massachusetts General Hospital, Harvard Medical School; MassGeneral Institute for Neurodegenerative Disease; Charlestown; MA; USA

6. Department of Neurology; College of Physicians and Surgeons; Columbia University; New York; NY; USA

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2012.03817.x/fullpdf

Reference13 articles.

1. Hematologically important mutations: Gaucher disease;Beutler;Blood Cells Mol Dis,2005

2. Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in European with Parkinson's disease;Lesage;Hum Mol Genet,2011

3. Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease;Sidransky;New Eng J Med,2009

4. Glucocerebrosidase gene mutations and Parkinson disease in the Norweigan population;Toft;Neurology,2006

5. New insights into the origin of the gaucher disease-causing mutation N370S: extended haplotype analysis using the 5GC3.2, 5470 G/A, and ITG6.2 polymorphisms;Rodríguez-Marí;Blood Cells Mol Dis,2001

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