Article

Novel mutation of NOTCH3 gene in a Chinese Patient with CADASIL: A case report

2024-08-26

Abstract excerpt

<title>Abstract</title> <p>Introduction: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a monogenic cerebral small-vessel disease characterized by migraine, recurrent ischemic strokes, psychiatric disorder, and progressive cognitive decline. CADASIL is a cerebrovascular disease closely related to the NOTCH3 gene and to date, over 300 mutations in this gene...

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Literature Corpus work: 40590f35-2a11-547b-aea9-8b96ab7e6b72
DOI: 10.21203/rs.3.rs-4795632/v1

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