Role of the VPS35 D620N mutation in Parkinson's disease-Reference-Cited by-同舟云学术

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Role of the VPS35 D620N mutation in Parkinson's disease

Published:2017-03 Issue: Volume:36 Page:10-18
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Mohan Megha^ORCID,Mellick George D.

Funder

Griffith University Postgraduate Research Scholarship

Parkinson's Queensland Incorporated PhD student grant

Publisher

Elsevier BV

Subject

Clinical Neurology,Geriatrics and Gerontology,Neurology

Reference102 articles.

1. An essay on the shaking palsy;Parkinson;J. Neuropsychiatry Clin. Neurosci.,2002

2. Clinical approach to Parkinson's disease: features, diagnosis, and principles of management;Massano;Cold Spring Harb. Perspect. Med.,2012

3. Parkinson's disease. First two parts;Lang;N Engl. J Med.,1998

4. Diagnostic criteria for Parkinson disease;Gelb;Arch. Neurol.,1999

5. Staging of brain pathology related to sporadic Parkinson's disease;Braak;Neurobiol. Aging,2003

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1. The Landscape of Monogenic Parkinson’s Disease in Populations of Non-European Ancestry: A Narrative Review;Genes;2023-11-17

2. The VINE complex is an endosomal VPS9-domain GEF and SNX-BAR coat;eLife;2022-08-08

3. Psychosis in Parkinson’s Disease: A Lesson from Genetics;Genes;2022-06-20

4. Autophagy and Parkinson’s Disease;Handbook of Neurotoxicity;2022

5. The VINE complex is a VPS9-domain GEF-containing SNX-BAR coat involved in endosomal sorting;2021-11-29

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