Skip to Main Content

Paper Details

Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
Acta Neurol Scand
5
2022
Arg133Cys, CADASIL, Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, Cys174Ser, Cys446Trp, Cys457Gly, Cys522Gly, Cys950Gly, Gly2035Argfs, NOTCH3 gene, NOTCH3 variants, Tyr1069Cys, c, c., c.1564T, c.397C, c.836A, cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, cerebral small vessel disease, patients
Author NameAffiliation
Johanna SchleutkerTurku University Hospital
Johanna SchleutkerInstitute of Biomedicine, University of Turku
Johanna SchleutkerTurku University Hospital
Johanna SchleutkerInstitute of Biomedicine, University of Turku
  • 1 - 4

Datasets

Release 1.2