Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

Hum Genet. 2005 Dec;118(3-4):543.
No abstract available

MeSH terms

  • Amino Acid Substitution
  • Cerebral Arterial Diseases / genetics*
  • Cerebral Infarction / etiology
  • Cerebral Infarction / genetics*
  • Codon, Nonsense
  • DNA Mutational Analysis
  • Dementia, Vascular / etiology
  • Dementia, Vascular / genetics*
  • Humans
  • Mutation, Missense*
  • Receptor, Notch3
  • Receptors, Notch / genetics*

Substances

  • Codon, Nonsense
  • NOTCH3 protein, human
  • Receptor, Notch3
  • Receptors, Notch