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Pathological changes and molecular ⁃ genetic mechanisms of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a inherited cerebral small vessel disease caused by Notch3 gene mutation. The molecular⁃genetic mechanisms of CADASIL have been still unclear. This review includes the physiopathology and gene mut...

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Principais autores: SUN Yuan⁃jing, FAN Yu⁃hua
Format: Artigo
Sprog:Inglês
Udgivet: Tianjin Huanhu Hospital 2021-10-01
Serier:Chinese Journal of Contemporary Neurology and Neurosurgery
Fag:
cadasil
receptor
notch3
pathology
molecular
review
Online adgang:http://www.cjcnn.org/index.php/cjcnn/article/view/2401
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