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Article

A new de novo Notch3 mutation causing CADASIL.

European journal of neurology - 1 Jun 2006

Coto E, Menéndez M, Navarro R, García-Castro M, Alvarez V

Abstract excerpt

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is one of the most common hereditary forms of stroke, and migraine with aura, mood disorders, or dementia, are also frequently found in these patients. Missense mutations in the Notch3 gene that c...

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Source

Identifiers

PMID: 16796587
DOI: 10.1111/j.1468-1331.2006.01337.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16796587-2026-09-02.1. Manifest publication-graph-cohort-2026-09-02.1.

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

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A new de novo Notch3 mutation causing CADASIL.PMID 16796587Read ↗

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A novel frameshift variant in the CADASIL gene NOTCH3: pathogenic or not?Semantic proximity Read ↗

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NOTCH3 gene mutations in subjects clinically suspected of CADASIL.Semantic proximity Read ↗

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