Associated Papers
TUBA4A: The Tale of an Unconventional Tubulin.
Zhu JL et al.
Cytoskeleton (hoboken, N.j.), 2025
Multiple roles for the cytoskeleton in ALS.
Liu X et al.
Experimental Neurology, 2022
Novel TUBA4A Variant Associated With Familial Frontotemporal Dementia.
Mol MO et al.
Neurology. Genetics, 2021
Discovery of coding regions in the human genome by integrated proteogenomics analysis workflow.
Zhu Y et al.
Nature Communications, 2018
29500430 (PubMed )
Supplement: 41467_2018_3311_MOESM5_ESM.xlsx › SAAVs_and_orthogonal_evidence
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations.
Pensato V et al.
Journal of Neurology, 2015
TUBA4A may not be a significant genetic factor in Chinese ALS patients.
Li J et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2015
Unraveling the multifaceted insights into amyotrophic lateral sclerosis: Genetic underpinnings, pathogenesis, and therapeutic horizons.
Sharma R et al.
Mutation Research. Reviews in Mutation Research, 0
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