SCARB2 variants and glucocerebrosidase activity in Parkinson’s disease-Reference-Cited by-同舟云学术

SCARB2 variants and glucocerebrosidase activity in Parkinson’s disease

Published:2016-03-10 Issue:1 Volume:2 Page:
ISSN:2373-8057
Container-title:npj Parkinson's Disease
language:en
Short-container-title:npj Parkinson's Disease

Author:

Alcalay Roy N,Levy Oren A,Wolf Pavlina,Oliva Petra,Zhang Xiaokui Kate,Waters Cheryl H,Fahn Stanley,Kang Un Jung,Liong Christopher,Ford Blair,Mazzoni Pietro,Kuo Sheng,Johnson Amelie,Xiong Lan,Rouleau Guy A,Chung Wendy K,Marder Karen S,Gan-Or Ziv

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Neurology

Link

http://www.nature.com/articles/npjparkd20164.pdf

Reference20 articles.

1. Sidransky, E. et al. Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. N. Engl. J. Med. 361, 1651–1661 (2009).

2. Neumann, J. et al. Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease. Brain 132, 1783–1794 (2009).

3. Zeigler, M. et al. A novel SCARB2 mutation in progressive myoclonus epilepsy indicated by reduced beta-glucocerebrosidase activity. J. Neurol. Sci. 339, 210–213 (2014).

4. Dardis, A. et al. Biochemical and molecular findings in a patient with myoclonic epilepsy due to a mistarget of the beta-glucosidase enzyme. Mol. Genet. Metab. 97, 309–311 (2009).

5. Do, C. B. et al. Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. PLoS Genet. 7, e1002141 (2011).

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