A Chinese CADASIL Family with a Novel Mutation on Exon 10 of Notch3 Gene

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), which is caused by the Notch3 gene mutation, has its unique clinical and imaging characteristics. Here we present a Chinese family with a novel mutation on exon 10 of Notch3 gene.

Source: Journal of Stroke and Cerebrovascular Diseases - June 10, 2021 Category: Neurology Authors: Yuan Liu, Shicun Huang, Liqiang Yu, Tan Li, Shanshan Diao, Zhiguo Chen, Guoqing Zhou, Xihua Sheng, Yuan Xu, Qi Fang Source Type: research