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A novel Notch3 deletion mutation in a Chinese patient with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL)

✍ Scribed by Weiming, Fan; Yuliang, Wang; Youjie, Li; Xinsheng, Liu; Shuyang, Xie; Zhaoxia, Liu

No coin nor oath required. For personal study only.

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