Controversial role of NOTCH3 gene cysteine sparing mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) phenotype: are they causative of the disease?

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作者： Cupidi, C. ^[1] ; Bernardi, L. ^[2] ; Clodomiro, A. ; Frangipane, F. ; Castagna, A. ; Puccio, G. ; Colao, R. ; Anfossi, M. ; Conidi, M. ; Gallo, M. ; Berti, G. ; Dotti, M. ; Federico, A. ; Maletta, R. ; Bruni, A.

作者单位： Univ Siena, Dept Neurol Neurosurg & Behav Sci, Unit Neurol Neurometab Dis, Via Laterina 8, I-53100 ^[1] ASP CZ, Reg Neurogenet Ctr CRN, Lamezia Terme, CZ, Czech Republic ^[2]

发布时间 2017-10-13

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Journal of Alzheimer's disease

2016年52卷Suppl.1期

S66-S67页

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Controversial role of NOTCH3 gene cysteine sparing mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) phenotype: are they causative of the disease?

Journal of Alzheimer's disease

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Journal of Alzheimer's disease

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Controversial role of NOTCH3 gene cysteine sparing mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) phenotype: are they causative of the disease?

Journal of Alzheimer's disease

相似文献

Journal of Alzheimer's disease

相关期刊

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