An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation
Published 2012 View Full Article
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Title
An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation
Authors
Keywords
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Journal
HUMAN MOLECULAR GENETICS
Volume 21, Issue 26, Pages 5484-5499
Publisher
Oxford University Press (OUP)
Online
2012-09-22
DOI
10.1093/hmg/dds393
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Note: Only part of the references are listed.- A novel mutation in the β-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance
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- (2010) Hillel Adesnik et al. NATURE
- Molecular Motors in Neurons: Transport Mechanisms and Roles in Brain Function, Development, and Disease
- (2010) Nobutaka Hirokawa et al. NEURON
- Wnt5a Induces Simultaneous Cortical Axon Outgrowth and Repulsive Axon Guidance through Distinct Signaling Mechanisms
- (2009) L. Li et al. JOURNAL OF NEUROSCIENCE
- Control of Cortical Axon Elongation by a GABA-Driven Ca2+/Calmodulin-Dependent Protein Kinase Cascade
- (2009) N. Ageta-Ishihara et al. JOURNAL OF NEUROSCIENCE
- Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria
- (2009) Xavier Hubert Jaglin et al. NATURE GENETICS
- Tubulin-related cortical dysgeneses: microtubule dysfunction underlying neuronal migration defects
- (2009) Xavier H. Jaglin et al. TRENDS IN GENETICS
- Abnormal development of the human cerebral cortex: genetics, functional consequences and treatment options
- (2008) Renzo Guerrini et al. TRENDS IN NEUROSCIENCES
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