Clinical Features of 4 Novel NOTCH3 Mutations of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy in China

BACKGROUND: This study aimed to identify NOTCH3 mutations and describe the genetic and clinical features and magnetic resonance imaging results in 11 unrelated patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) from Henan province in Ch...

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Detalles Bibliográficos
Autores principales: Qin, Weiwei, Ren, Zhixia, Xia, Mingrong, Yang, Miaomiao, Shi, Yingying, Huang, Yue, Guo, Xiangqian, Zhang, Jiewen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2019
Materias:
Human Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6778411/
https://www.ncbi.nlm.nih.gov/pubmed/31554780
http://dx.doi.org/10.12659/MSMBR.918830

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