Four novel optineurin mutations in patients with sporadic amyotrophic lateral sclerosis in Mainland China
Author:
Funder
National Natural Science Foundation of China
Publisher
Elsevier BV
Subject
Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience
Reference37 articles.
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2. A Dutch family with autosomal recessively inherited lower motor neuron predominant motor neuron disease due to optineurin mutations;Beeldman;Amyotroph. Lateral Scler. Frontotemporal Degener.,2015
3. Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis;Belzil;Neurobiol. Aging,2011
4. El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis;Brooks;Amyotroph. Lateral Scler. Other Motor Neuron Disord.,2009
5. Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions of C9ORF72-ALS;Bury;Neuropathology,2016
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1. Physiological and pathological effects of phase separation in the central nervous system;Journal of Molecular Medicine;2024-03-05
2. Molecular Chaperones’ Potential against Defective Proteostasis of Amyotrophic Lateral Sclerosis;Cells;2023-05-02
3. Presence of Rare Variants is Associated with Poorer Survival in Chinese Patients with Amyotrophic Lateral Sclerosis;Phenomics;2023-02-12
4. Prove pathogenicity of OPTN variants before establishing a causal relation with amyotrophic lateral sclerosis;Neurobiology of Aging;2021-10
5. Authors’ reply: Four novel optineurin mutations in patients with sporadic amyotrophic lateral sclerosis in Mainland China;Neurobiology of Aging;2021-08
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