Most common NOTCH3 mutations causing CADASIL or CADASIL-like cerebral small vessel disease: A systematic review

Most common NOTCH3 mutations causing CADASIL or CADASIL-like cerebral small vessel disease: A systematic review

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is a monogenic disorder caused by mutations in the NOTCH3 gene. The main aim of our survey was to determine if there is an association between phenotypes and genotypes across the most common NOTCH3 m...

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Bibliographic Details
Main Authors: Georgina Boston, Dan Jobson, Toshiki Mizuno, Masafumi Ihara, Raj N Kalaria
Format: Article
Language:English
Published: Elsevier 2024-01-01
Series:Cerebral Circulation - Cognition and Behavior
Subjects:
CADASIL
Dementia
NOTCH3
Mutation
Phenotype
Online Access:http://www.sciencedirect.com/science/article/pii/S266624502400028X

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http://www.sciencedirect.com/science/article/pii/S266624502400028X

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