A new de novo Notch3 mutation causing CADASIL
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2006.01337.x/fullpdf
Reference17 articles.
1. Clinical spectrum of CADASIL: a study of 7 families
2. CADASIL: a Common Form of Hereditary Arteriopathy Causing Brain Infarcts and Dementia
3. Notch signaling and inherited disease syndromes
4. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
5. Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients
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2. Exome-based gene panel analysis in a cohort of acute juvenile ischemic stroke patients:relevance of NOTCH3 and GLA variants;Journal of Neurology;2022-11-21
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5. Contribution of “Omic” Studies to the Understanding of Cadasil. A Systematic Review;International Journal of Molecular Sciences;2021-07-08
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