Associated Papers
Characterising the Genetic Landscape of Amyotrophic Lateral Sclerosis: A Catalogue and Assessment of Over 1,000 Published Genetic Variants.
McCann EP et al.
Journal of Neuromuscular Diseases, 2023
37638449 (PubMed )
Supplement: jnd-10-jnd230148-s001.xlsx › variant_list
The role of sequestosome 1/p62 protein in amyotrophic lateral sclerosis and frontotemporal dementia pathogenesis.
Foster AD et al.
Neural Regeneration Research, 2020
The role of Nrf2 signaling in counteracting neurodegenerative diseases.
Dinkova-Kostova AT et al.
The Febs Journal, 2018
[Association between VAPB mutations and familial amyotrophic lateral sclerosis in Chinese patients].
Zhang H et al.
Zhonghua Yi Xue Za Zhi, 2015
Six SQSTM1 mutations in a Chinese amyotrophic lateral sclerosis cohort.
Yang Y et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2015
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