Novel human pathological mutations. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant aretriopathy with subcortical infarcts and leukoencephalopathy
Hum Genet
.
2007 Jun;121(5):651-2.
Authors
Susana Ferreira
1
,
Filipa Malheiro
,
João Paulo Oliveira
Affiliation
1
Faculdade de Medicina, Universade do Porto, Serviço de Genética Médica, and Hospital Egas Moniz, Lisboa, Portugal. susanadg@med.up.pt
PMID:
17879453
No abstract available
MeSH terms
Brain Diseases / genetics*
Genes, Dominant*
Humans
Mutation
Receptor, Notch3
Receptors, Notch / genetics*
Substances
NOTCH3 protein, human
Receptor, Notch3
Receptors, Notch