Associated Papers
Variability in Clinical Phenotype in TARDBP Mutations: Amyotrophic Lateral Sclerosis Case Description and Literature Review.
Lombardi M et al.
Genes, 2023
38002982 (PubMed )
Supplement: genes-14-02039-s001.zip › genes-2688630-supplementary › genes-2688630.xlsx › 267_paz
Genetic and clinical features of Chinese sporadic amyotrophic lateral sclerosis patients with TARDBP mutations.
Feng F et al.
Brain and Behavior, 2021
High frequency of the TARDBP p.M337 V mutation among south-eastern Chinese patients with familial amyotrophic lateral sclerosis.
Xu GR et al.
Bmc Neurology, 2018
Genetic analysis of patients with familial and sporadic amyotrophic lateral sclerosis in a Brazilian Research Center.
Chadi G et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2017
27978769 (PubMed )
Supplement: supplement_1.pdf
Screening of the TARDBP gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin.
Zou ZY et al.
Neurobiology of Aging, 2012
TARDBP gene mutations among Chinese patients with sporadic amyotrophic lateral sclerosis.
Huang R et al.
Neurobiology of Aging, 2012
Large-scale screening of TARDBP mutation in amyotrophic lateral sclerosis in Japanese.
Iida A et al.
Neurobiology of Aging, 2012
Association between novel TARDBP mutations and Chinese patients with amyotrophic lateral sclerosis.
Xiong HL et al.
Bmc Medical Genetics, 2010
Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis.
Kamada M et al.
Journal of the Neurological Sciences, 2009
Select a paper to view details