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CADASIL: case report

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is a hereditary cerebral arteriopathy caused by mutations in the Notch-3 gene. The diagnosis is reached by skin biopsy revealing presence of granular osmiophílic material (GOM), and/or by genetic tes...

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Detalles Bibliográficos
Autores principales:	da Silva, Julio Cesar Vasconcelos, Gasparetto, Emerson L., Engelhardt, Eliasz
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Associação de Neurologia Cognitiva e do Comportamento 2012
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618968/ https://www.ncbi.nlm.nih.gov/pubmed/29213795 http://dx.doi.org/10.1590/S1980-57642012DN06030013

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