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A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse
Human cortical malformations, including lissencephaly, polymicrogyria and other diseases of neurodevelopment, have been associated with mutations in microtubule subunits and microtubule-associated proteins. Here we report our cloning of the brain dimple (brdp) mouse mutation, which we recovered from...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3781635/ https://ncbi.nlm.nih.gov/pubmed/23727838 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddt255 |
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