Proyecto
 (2017)

Clinical, imaging, histological and genetic characterization of a family with CADASIL in CHILE.

Matamala, Jose Manuel; Sánchez, Carolina; Gallardo, Andrés; Fonseca, Beatriz

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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.