Clinical Features of 4 Novel NOTCH3 Mutations of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy in China-Reference-Cited by-同舟云学术

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

Published:2019-09-26 Issue: Volume:25 Page:199-209
ISSN:2325-4416
Container-title:Medical Science Monitor Basic Research
language:en
Short-container-title:Med Sci Monit Basic Res

Author:

Qin Weiwei¹,Ren Zhixia¹,Xia Mingrong¹,Yang Miaomiao¹,Shi Yingying¹,Huang Yue¹,Guo Xiangqian²,Zhang Jiewen¹

Affiliation:

1. Department of Neurology, State Key Clinical Specialty of the Ministry of Health for Neurology, Henan Provincial People’s Hospital, School of Clinical Medicine, Henan University, Zhengzhou, Henan, China (mainland)

2. Department of Biochemistry and Molecular Biology, Medical School of Henan University, Kaifeng, Henan, China (mainland)

Publisher

International Scientific Information, Inc.

Subject

General Medicine

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mutation spectrum and genotype–phenotype correlations in 157 Korean CADASIL patients: a multicenter study;neurogenetics;2021-11-06

2. A Chinese CADASIL family with p.R578C mutation at exon 11 of the NOTCH3 gene;Clinical Neurology and Neurosurgery;2021-09

3. NOTCH3 Variants and Genotype-Phenotype Features in Chinese CADASIL Patients;Frontiers in Genetics;2021-07-15

4. The role of NOTCH3 variants in Alzheimer's disease and subcortical vascular dementia in the Chinese population;CNS Neuroscience & Therapeutics;2021-05-04

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