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Disease-associated mutations in human TUBB3 disturb netrin repulsive signaling
Missense mutations in the human TUBB3 gene cause a variety of neurological disorders associated with defects in axon guidance and neuronal migration, but the underlying molecular mechanisms are not well understood. Recent studies have shown that direct coupling of dynamic TUBB3 in microtubules with...
Tallennettuna:
| Julkaisussa: | PLoS One |
|---|---|
| Päätekijät: | , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Public Library of Science
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6588280/ https://ncbi.nlm.nih.gov/pubmed/31226147 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0218811 |
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