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TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on tubulins
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Mutations in the tubulin gene TUBB2B result in asymmetrical polymicrogyria
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Evidence of an asymmetrical endophenotype in congenital fibrosis of extraocular muscles type 3 resulting from TUBB3 mutations
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Demer, J. L., Clark, R. A., Tischfield, M. A., and Engle, E. C. (2010) Evidence of an asymmetrical endophenotype in congenital fibrosis of extraocular muscles type 3 resulting from TUBB3 mutations. Invest. Ophthalmol. Vis. Sci. 51, 4600-4611
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Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance
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Mutations in the neuronal-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects
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Mutations in the autoregulatory domain of tubulin 4a cause hereditary dystonia
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