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