QuickView for CCM2;jsessionid=79A978B19B1A0980BF22C8D398C061DC;jsessionid=5A11652EF3428229AD18DD23F6B5EE99;jsessionid=B5723C39781E916B675001AC72F7438C;jsessionid=0C787BBE50802756A462FD3D83A74091 (gene)

1. Alternatively spliced isoforms reveal a novel type of PTB domain in CCM2 protein.
2. CCM2-deficient endothelial cells undergo a ROCK-dependent reprogramming into senescence-associated s…
3. Familial cerebral cavernous malformation presenting with epilepsy caused by mutation in the CCM2 gen…
4. First Report of Concomitant Pathogenic Mutations Within MGC4607/CCM2 and KRIT1/CCM1 in a Familial Ce…
5. Novel CCM2 missense variants abrogating the CCM1-CCM2 interaction cause cerebral cavernous malformat…

There were no clinical trials for CCM2;jsessionid=79A978B19B1A0980BF22C8D398C061DC;jsessionid=5A11652EF3428229AD18DD23F6B5EE99;jsessionid=B5723C39781E916B675001AC72F7438C;jsessionid=0C787BBE50802756A462FD3D83A74091