De novo mutation in the NOTCH3 gene causing CADASIL

De novo mutation in the NOTCH3 gene causing CADASIL

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is one of the most common hereditary forms of stroke, and migraine with aura, mood disorders and dementia. CADASIL is caused by mutations of the NOTCH3 gene. This mutation is inherited as an autosom...

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Bibliographic Details
Main Authors: Dragan Stojanov, Danijela Grozdanović, Sladjana Petrović, Daniela Benedeto-Stojanov, Ivan Stefanović, Nebojša Stojanović, Dušica N. Ilić
Format: Article
Language:English
Published: Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina 2014-05-01
Series:Biomolecules & Biomedicine
Subjects:
CADASIL
NOTCH3 gene
de novo mutation
CT
Online Access:https://www.bjbms.org/ojs/index.php/bjbms/article/view/2297

Internet

https://www.bjbms.org/ojs/index.php/bjbms/article/view/2297

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