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  • Title: [From gene to disease; from Notch3 to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].
    Author: Oberstein SA, Bakker E, Ferrari MD, Haan J.
    Journal: Ned Tijdschr Geneeskd; 2001 Feb 24; 145(8):359-60. PubMed ID: 11257815.
    Abstract:
    Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy' (CADASIL) is an autosomal dominant inherited arteriopathy leading to brain infarcts and dementia at middle age with extensive cerebral white matter changes on MRI. CADASIL is caused by mutations in the Notch3 gene on chromosome 19.
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