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Chd7 Cooperates with Sox10 and Regulates the Onset of CNS Myelination and Remyelination
Mutations in CHD7, encoding ATP-dependent chromodomain-helicase-DNA-binding protein 7, in CHARGE syndrome leads to multiple congenital anomalies including craniofacial malformations, neurological dysfunction and growth delay. Currently, mechanisms underlying the CNS phenotypes remain poorly understo...
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| Publicat a: | Nat Neurosci |
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| Autors principals: | , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4846514/ https://ncbi.nlm.nih.gov/pubmed/26928066 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nn.4258 |
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