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RAB18, a protein associated with Warburg Micro syndrome, controls neuronal migration in the developing cerebral cortex
BACKGROUND: Loss of function mutations in RAB18, has been identified in patients with the human neurological and developmental disorder Warburg Micro syndrome. However, the function of RAB18 in brain remains unknown. RESULTS: In this study, we report that RAB18 is a critical regulator of neuronal mi...
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| Publicado no: | Mol Brain |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4754921/ https://ncbi.nlm.nih.gov/pubmed/26879639 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13041-016-0198-2 |
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