Associated Papers
C21ORF2 mutations point towards primary cilia dysfunction in amyotrophic lateral sclerosis.
De Decker M et al.
Brain : a Journal of Neurology, 2025
Emerging roles of primary cilia in the pathogenesis of amyotrophic lateral sclerosis.
Takahashi H et al.
Frontiers in Neuroscience, 2025
Prediction of structural consequences for disease causing variants in C21orf2 protein using computational approaches.
Iyer S et al.
Journal of Biomolecular Structure & Dynamics, 2019
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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