The comparisons of phenotype and genotype between CADASIL and CADASIL-like patients and population-specific evaluation of CADASIL scale in China

BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common form of hereditary stroke disorder caused by mutations in the NOTCH3 gene. Although CADASIL scale is a widely used tool to screen clinically suspected CADASIL patients,...

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Detalles Bibliográficos
Autores principales: He, Dan, Chen, Daiqi, Li, Xuefei, Hu, Zheng, Yu, Zhiyuan, Wang, Wei, luo, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4875019/
https://www.ncbi.nlm.nih.gov/pubmed/27206574
http://dx.doi.org/10.1186/s10194-016-0646-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4875019/
https://www.ncbi.nlm.nih.gov/pubmed/27206574
http://dx.doi.org/10.1186/s10194-016-0646-5

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