Molecular genetic features and clinical manifestations in Chinese familial cerebral cavernous malformation: from a novel KRIT1/CCM1 mutation (c.1119dupT) to an overall view
Article in Frontiers in Neuroscience (May 2023)
The most recent citing publications are shown below. View all 4 publications that cite this research output on Dimensions.
A Chinese Family With Cerebral Cavernous Malformation Caused by a Frameshift Mutation of the CCM1 Gene: A Case Report and Review of the Literature
Article in Frontiers in Neurology (April 2022)
In-silico analysis of nonsynonymous genomic variants within CCM2 gene reaffirm the existence of dual cores within typical PTB domain
Article in Biochemistry and Biophysics Reports (January 2022)