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Article

NOTCH3 mutations and clinical features in 33 mainland Chinese families with CADASIL.

Journal of neurology, neurosurgery, and psychiatry - 1 May 2011

Wang Zhaoxia, Yuan Yun, Zhang Wei, Lv He, Hong Daojun, Chen Bin, Liu Yang, Luan Xinghua, Xie Sheng, Wu Shiwen

Abstract excerpt

BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is an inherited small-vessel disease caused by mutations in NOTCH3. Although CADASIL cases have been identified worldwide, the data from mainland China are still limited. OBJECTIVE: To...

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Source

Identifiers

PMID: 20935329
DOI: 10.1136/jnnp.2010.209247

Genes

NOTCH3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20935329-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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