Identification of a Novel CCM1 Frameshift Mutation in a Chinese Han Family With Multiple Cerebral Cavernous Malformations
Author:
Publisher
Frontiers Media SA
Subject
General Neuroscience
Reference50 articles.
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1. 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
2. Case Report: A novel heterozygous nonsense mutation in KRIT1 cause hereditary cerebral cavernous malformation;Frontiers in Oncology;2023-04-27
3. Advances in differential diagnosis of cerebrovascular diseases in magnetic resonance imaging: a narrative review;Quantitative Imaging in Medicine and Surgery;2023-04
4. A familiar cerebral cavernous malformations (FCCMs) patient with CCM1 deletion-frameshift mutation generates an induced pluripotent stem cell line (NFHHMUi001-A);Stem Cell Research;2022-08
5. A Chinese Family With Cerebral Cavernous Malformation Caused by a Frameshift Mutation of the CCM1 Gene: A Case Report and Review of the Literature;Frontiers in Neurology;2022-04-04
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