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Mutant Ahi1 Affects Retinal Axon Projection in Zebrafish via Toxic Gain of Function
Joubert syndrome (JBTS) is an inherited autosomal recessive disorder associated with cerebellum and brainstem malformation and can be caused by mutations in the Abelson helper integration site-1 (AHI1) gene. Although AHI1 mutations in humans cause abnormal cerebellar development and impaired axonal...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438259/ https://www.ncbi.nlm.nih.gov/pubmed/30949029 http://dx.doi.org/10.3389/fncel.2019.00081 |