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Novel human pathological mutations. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).

Human genetics - 1 Jun 2007

Ferreira Susana, Silva Rosa S, Oliveira João Paulo

Abstract excerpt

No abstract is available from the source.

Topics

CADASIL
Humans
Mutation
Receptor, Notch3
Receptors, Notch

Source

Identifiers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

PMID: 17879446

Genes

NOTCH3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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Novel human pathological mutations. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).PMID 17879446Read ↗

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