A Pachygyria-causing α-Tubulin Mutation Results in Inefficient Cycling with CCT and a Deficient Interaction with TBCB

The agyria (lissencephaly)/pachygyria phenotypes are catastrophic developmental diseases characterized by abnormal folds on the surface of the brain and disorganized cortical layering. In addition to mutations in at least four genes—LIS1, DCX, ARX and RELN—mutations in a human α-tubulin gene, TUBA1A...

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Main Authors: Tian, Guoling, Kong, Xiang-Peng, Jaglin, Xavier H., Chelly, Jamel, Keays, David, Cowan, Nicholas J.
Formato: Artigo
Idioma:Inglês
Publicado: The American Society for Cell Biology 2008
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Articles
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC2262973/
https://ncbi.nlm.nih.gov/pubmed/18199681
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1091/mbc.E07-09-0861
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