Varaico: Literature-Extracted Genetic Variants

Gene:TUBB3
Variant:p.R391H
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TUBB3

NM_006086.4:p.R391H

Associated Papers

Monogenic defects in Russian children with autism spectrum disorders.

Suspitsin EN et al.

World Journal of Clinical Pediatrics, 2025

R391 human dominant mutation does not affect TubB4b localization and sensory hair cells structure in zebrafish inner ear and lateral line.

Smaili W et al.

Developmental Biology, 2025

The emerging role of the tubulin code: From the tubulin molecule to neuronal function and disease.

Chakraborti S et al.

Cytoskeleton (hoboken, N.j.), 2016

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."