Absence of Mutations in Exon 6 of the TARDBP Gene in 207 Chinese Patients with Sporadic Amyotrohic Lateral Sclerosis
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference13 articles.
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1. Genotype–phenotype association of TARDBP mutations in Chinese patients with amyotrophic lateral sclerosis: a single-center study and systematic review of published literature;Journal of Neurology;2022-03-03
2. Genetic and clinical features of Chinese sporadic amyotrophic lateral sclerosis patients with TARDBP mutations;Brain and Behavior;2021-08
3. The Role of TDP-43 in Genome Repair and beyond in Amyotrophic Lateral Sclerosis;Amyotrophic Lateral Sclerosis - Recent Advances and Therapeutic Challenges;2020-08-26
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5. High frequency of the TARDBP p.M337 V mutation among south-eastern Chinese patients with familial amyotrophic lateral sclerosis;BMC Neurology;2018-04-05
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