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notch3 is essential for oligodendrocyte development and vascular integrity in zebrafish
Mutations in the human NOTCH3 gene cause CADASIL syndrome (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy). CADASIL is an inherited small vessel disease characterized by diverse clinical manifestations including vasculopathy, neurodegeneration and dementia...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Company of Biologists Limited
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3759344/ https://ncbi.nlm.nih.gov/pubmed/23720232 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.012005 |
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