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Clinical, imaging, histological and genetic characterization of a family with CADASIL in CHILE.
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| Fecha de publicación: | 2017 |
| Año de Inicio/Término: | 2017-2018 |
| Financiamiento/Sponsor: | Universidad de Chile |
| Notas: | The autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an arteriopathy caused by a mutation in the Notch3 gene. We found two SNPs in exons 3 and 4, which could be associated with the disease. |