Genetic and clinical features of Chinese sporadic amyotrophic lateral sclerosis patients with TARDBP mutations

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High frequency of the TARDBP p.M337 V mutation among south-eastern Chinese patients with familial amyotrophic lateral sclerosis

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Two distinct clinical features and cognitive impairment in amyotrophic lateral sclerosis patients with TARDBP gene mutations in the Chinese population

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Absence of Mutations in Exon 6 of the TARDBP Gene in 207 Chinese Patients with Sporadic Amyotrohic Lateral Sclerosis

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Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations

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Association between novel TARDBP mutations and Chinese patients with amyotrophic lateral sclerosis

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Mutational analysis of TARDBP in neurodegenerative diseases

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