Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA pathogenic rare mutation on exon 22 of the NOTCH3 gene disclosed in an Italian patient affected by CADASIL.AuthorsUngaro, C.; Servillo, P.; Mazzei, Rosalucia; Consoli, D.; Conforti, F.; Sprovieri, T.; Lanza, P.; Quattrone, A.AbstractA letter to the editor is presented regarding a case of a 55-year-old woman with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL).SubjectsLETTERS to the editor; NEUROPSYCHOLOGYPublicationNeurological Sciences, 2009, Vol 30, Issue 3, p269ISSN1590-1874Publication typeLetterDOI10.1007/s10072-009-0040-z