New mutations in the Notch3 gene in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL)

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作者： Abramycheva, Natalya ^[1] ; Stepanova, Maria ^[2] ; Kalashnikova, Lyudmila ^[3] ; Zakharova, Maria ^[4] ; Maximova, Marina ^[5] ; Tanashyan, Marine ^[6] ; Lagoda, Olga ^[7] ; Fedotova, Ekaterina ; Klyushnikov, Sergey ; Konovalov, Rodion ; Sakharova, Alla ; Illarioshkin, Sergey

作者单位： Russian Acad Med Sci, Res Ctr Neurol, Dept Demyelinating Dis, Moscow 125367, Russia ^[1] Russian Acad Med Sci, Res Ctr Neurol, Dept Pathol, Moscow 125367, Russia ^[2] Russian Acad Med Sci, Res Ctr Neurol, Dept Acute Stroke, Intens Care Unit, Moscow 125367, Russia ^[3] Russian Acad Med Sci, Res Ctr Neurol, Dept Neuroradiol, Moscow 125367, Russia ^[4] Russian Acad Med Sci, Res Ctr Neurol, Dept Neurogenet, Moscow 125367, Russia ^[5] Russian Acad Med Sci, Res Ctr Neurol, Dept Neurorehabil, Moscow 125367, Russia ^[6] Russian Acad Med Sci, Res Ctr Neurol, Dept Chron Cerebrovasc Dis, Moscow 125367, Russia ^[7]

关键词 CADASIL White matter lesions NOTCH3 gene Mutations Phenotypic heterogeneity Russian population

发布时间 2017-04-06

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