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Genetic spectrum of NOTCH3 and clinical phenotype of CADASIL patients in different populations

INTRODUCTION: Cerebral autosomal‐dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a relatively common cerebral small vessel disease. NOTCH3 has been identified as the causative gene of CADASIL. Clinical variability and genetic heterogeneity were observed in CADASI...

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Detalles Bibliográficos
Autores principales:	Ni, Wang, Zhang, Yi, Zhang, Liang, Xie, Juan‐Juan, Li, Hong‐Fu, Wu, Zhi‐Ying
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9532899/ https://www.ncbi.nlm.nih.gov/pubmed/35822697 http://dx.doi.org/10.1111/cns.13917

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