The relationship between glucocerebrosidase mutations and Parkinson disease-Reference-Cited by-同舟云学术

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The relationship between glucocerebrosidase mutations and Parkinson disease

Published:2016-02-10 Issue: Volume:139 Page:77-90
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:J. Neurochem.

Author:

Migdalska-Richards Anna¹,Schapira Anthony H. V.¹

Affiliation:

1. Department of Clinical Neurosciences; UCL Institute of Neurology; London UK

Funder

Medical Research Council

Javon Trust

Parkinson's UK (PUK)

National Institute for Health Research

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jnc.13385/fullpdf

Reference125 articles.

1. Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews;Aharon-Peretz;N. Engl. J. Med.,2004

2. Chaperone-mediated autophagy markers in Parkinson disease brains;Alvarez-Erviti;Arch. Neurol.,2010

3. Genotype and phenotype in Parkinson's disease: lessons in heterogeneity from deep brain stimulation;Angeli;Mov. Disord.,2013

4. Glucocerebrosidase mutations in primary parkinsonism;Asselta;Parkinsonism Relat. Disord.,2014

5. Evolution of prodromal clinical markers of Parkinson disease in a GBA mutation-positive cohort;Beavan;JAMA Neurol.,2015

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