Genetic spectrum of <scp> <i>NOTCH3</i> </scp> and clinical phenotype of <scp>CADASIL</scp> patients in different populations-Reference-Cited by-同舟云学术

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

Published:2022-07-13 Issue:11 Volume:28 Page:1779-1789
ISSN:1755-5930
Container-title:CNS Neuroscience & Therapeutics
language:en
Short-container-title:CNS Neurosci Ther

Author:

Ni Wang¹,Zhang Yi¹,Zhang Liang¹,Xie Juan‐Juan¹,Li Hong‐Fu¹^ORCID,Wu Zhi‐Ying¹^ORCID

Affiliation:

1. Department of Neurology and Department of Medical Genetics in the Second Affiliated Hospital, and Key Laboratory of Medical Neurobiology of Zhejiang Province Zhejiang University School of Medicine Hangzhou China

Publisher

Wiley

Subject

Pharmacology (medical),Physiology (medical),Psychiatry and Mental health,Pharmacology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cns.13917

Reference25 articles.

1. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

2. CADASIL and CARASIL

3. The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients

4. Notch3 Signaling and Aggregation as Targets for the Treatment of CADASIL and Other NOTCH3-Associated Small-Vessel Diseases

5. Imaging Characteristics of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy (CADASIL)

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