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The Joubert Syndrome Gene arl13b is Critical for Early Cerebellar Development in Zebrafish
Joubert syndrome is characterized by unique malformation of the cerebellar vermis. More than thirty Joubert syndrome genes have been identified, including ARL13B. However, its role in cerebellar development remains unexplored. We found that knockdown or knockout of arl13b impaired balance and locomo...
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| Опубликовано в: : | Neurosci Bull |
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| Главные авторы: | , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Springer Singapore
2020
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7475164/ https://ncbi.nlm.nih.gov/pubmed/32812127 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12264-020-00554-y |
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