Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalActa Neurologica Scandinavica
Volume146
Issue number5
Pages (from-to)643-651
Number of pages9
ISSN0001-6314
DOIs
Publication statusPublished - Nov 2022
MoE publication typeA1 Journal article-refereed

Fields of Science

  • CADASIL
  • Finnish
  • genotype
  • mutation
  • NOTCH3
  • phenotype
  • MUTATIONS
  • PREVALENCE
  • 3112 Neurosciences
  • 3124 Neurology and psychiatry

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