Novel human pathological mutations. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL)
Hum Genet
.
2007 Jun;121(5):649.
Authors
Susana Ferreira
1
,
Cristina Costa
,
João Paulo Oliveira
Affiliation
1
Faculdade de Medicina, Universidade do Porto, Serviço de Genética Médica, Portugal.
[email protected]
PMID:
17879445
No abstract available
MeSH terms
CADASIL / genetics*
Humans
Mutation*
Receptor, Notch3
Receptors, Notch / genetics*
Substances
NOTCH3 protein, human
Receptor, Notch3
Receptors, Notch