A Chinese Family With Cerebral Cavernous Malformation Caused by a Frameshift Mutation of the CCM1 Gene: A Case Report and Review of the Literature

Overview of attention for article published in Frontiers in Neurology, April 2022

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New Research: A Chinese Family With Cerebral Cavernous Malformation Caused by a Frameshift Mutation of the CCM1 Gene: A Case Report and Review of the Literature: Background Familial cerebral cavernous malformation (FCCM) is a vascular… https://t.co/sqmwQ9

04 Apr 2022

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