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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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| Vydáno v: | Mol Brain |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2016
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| Témata: | |
| On-line přístup: | 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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