notch3 is essential for oligodendrocyte development and vascular integrity in zebrafish
SUMMARY 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...
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| Main Authors: | , , , , |
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| Format: | Book |
| Published: |
The Company of Biologists,
2013-09-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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