Plasma Glucosylsphingosine in GBA1 Mutation Carriers with and without Parkinson's Disease-Reference-Cited by-同舟云学术

Plasma Glucosylsphingosine in GBA1 Mutation Carriers with and without Parkinson's Disease

Published:2021-11-06 Issue: Volume: Page:
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Movement Disorders

Author:

Surface Matthew¹,Balwani Manisha²,Waters Cheryl¹,Haimovich Alexander¹,Gan‐Or Ziv³⁴⁵^ORCID,Marder Karen S.¹,Hsieh Tammy⁶,Song Linxia⁶,Padmanabhan Shalini⁷^ORCID,Hsieh Frank⁶,Merchant Kalpana M.⁸,Alcalay Roy N.¹^ORCID

Affiliation:

1. Department of Neurology, College of Physicians and Surgeons Columbia University New York New York USA

2. Department of Genetics and Genomic Sciences Icahn School of Medicine at Mount Sinai New York New York USA

3. The Neuro (Montreal Neurological Institute‐Hospital) McGill University Montreal Quebec Canada

4. Department of Neurology and Neurosurgery McGill University Montreal Quebec Canada

5. Department of Human Genetics McGill University Montreal Quebec Canada

6. Nextcea, Inc. Woburn Massachusetts USA

7. The Michael J. Fox Foundation for Parkinson's Research New York New York USA

8. Northwestern University Feinberg School of Medicine Chicago Illinois USA

Funder

Michael J. Fox Foundation for Parkinson's Research

National Institute of Neurological Disorders and Stroke

Parkinson's Foundation

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.28846

Reference29 articles.

1. Gaucher disease: mutation and polymorphism spectrum in the glucocerebrosidase gene (GBA)

2. Occurrence of Parkinson's syndrome in type 1 Gaucher disease

3. Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

4. Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset

5. Gaucher Disease Glucocerebrosidase and α-Synuclein Form a Bidirectional Pathogenic Loop in Synucleinopathies

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