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Human TUBB3 Mutations Disrupt Netrin Attractive Signaling
Heterozygous missense mutations in human TUBB3 gene result in a spectrum of brain malformations associated with defects in axon guidance, neuronal migration and differentiation. However, the molecular mechanisms underlying mutation-related axon guidance abnormalities are unclear. Recent studies have...
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| 出版年: | Neuroscience |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5841466/ https://ncbi.nlm.nih.gov/pubmed/29382549 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroscience.2018.01.046 |
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