A Novel CCM2 Gene Mutation Associated With Cerebral Cavernous Malformation
Author:
Publisher
Frontiers Media SA
Subject
Clinical Neurology,Neurology
Reference38 articles.
1. Novel KRIT1/CCM1 and MGC4607/CCM2 gene variants in Chinese families with cerebral cavernous malformations;Wang;Front Neurol,2018
2. Cerebral cavernous malformations: an update on prevalence, molecular genetic analyses, and genetic counselling;Spiegler;Mol Syndromol,2018
3. Genetics of cavernous angiomas;Labauge;Lancet Neurol.,2007
4. Cerebral cavernous malformations: from genes to proteins to disease;Cavalcanti;J Neurosurg.,2012
5. Cerebral cavernous malformations: from molecular pathogenesis to genetic counselling and clinical management;Haasdijk;Eur J Hum Genet.,2012
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1. Peripheral macrophages in the development and progression of structural cerebrovascular pathologies;Journal of Cerebral Blood Flow & Metabolism;2023-11-24
2. Molecular genetic features and clinical manifestations in Chinese familial cerebral cavernous malformation: from a novel KRIT1/CCM1 mutation (c.1119dupT) to an overall view;Frontiers in Neuroscience;2023-05-05
3. A novel KRIT1/CCM1 mutation accompanied by a NOTCH3 mutation in a Chinese family with multiple cerebral cavernous malformations;neurogenetics;2023-03-09
4. The Genetic Architecture of Vascular Anomalies: Current Data and Future Therapeutic Perspectives Correlated with Molecular Mechanisms;International Journal of Molecular Sciences;2022-10-13
5. In-silico analysis of nonsynonymous genomic variants within CCM2 gene reaffirm the existence of dual cores within typical PTB domain;Biochemistry and Biophysics Reports;2022-03
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