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Novel mutation of the notch3 gene in arabic family with CADASIL
Mutations in the NOTCH3 gene are responsible for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), an adult onset hereditary angiopathy leading to ischemic stroke, vascular dementia and psychiatric disorders. All mutation of NOTCH3 described so far...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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PAGEPress Publications
2011
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207232/ https://www.ncbi.nlm.nih.gov/pubmed/22053260 http://dx.doi.org/10.4081/ni.2011.e6 |