Valosin-containing-protein pathogenic variant p.R487H in Parkinson’s disease-Reference-Cited by-同舟云学术

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Valosin-containing-protein pathogenic variant p.R487H in Parkinson’s disease

Published:2024 Issue: Volume:10 Page:100236
ISSN:2590-1125
Container-title:Clinical Parkinsonism & Related Disorders
language:en
Short-container-title:Clinical Parkinsonism & Related Disorders

Author:

Piat Capucine,Ross Owen A.,Springer Wolfdieter,Benarroch Eduardo E.,Layne Moore J.,Lauer Emily,Niu Zhiyv,Savica Rodolfo^ORCID

Funder

American Academy of Neurology

National Institute of Diabetes and Digestive and Kidney Diseases

American Parkinson Disease Association

National Institute of Neurological Disorders and Stroke

BrightFocus Foundation

National Institute on Aging

ACADIA Pharmaceuticals

National Heart, Lung, and Blood Institute

Ted Nash Long Life Foundation

Michael J. Fox Foundation for Parkinson's Research

Publisher

Elsevier BV

Reference5 articles.

1. Exome sequencing reveals VCP mutations as a cause of familial ALS;Johnson;Neuron,2010

2. Multisystem proteinopathy due to VCP mutations: A review of clinical heterogeneity and genetic diagnosis;Pfeffer;Genes (Basel),2022

3. 215th ENMC International Workshop VCP-related multi-system proteinopathy (IBMPFD) 13-15 November 2015, Heemskerk, The Netherlands;Evangelista;Neuromuscul. Disord.,2016

4. Valosin-containing protein mutation and Parkinson's disease;Chan;Parkinsonism Relat. Disord.,2012

5. VCP expression decrease as a biomarker of preclinical and early clinical stages of Parkinson's disease;Alieva;Sci. Rep.,2020

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