CCM1Cerebral Cavernous Malformation Type 1
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CCM1 mutation screen of sporadic cases with cerebral cavernous malformations.
It was already known that the disease develops when the CCM1 gene is inactive in endothelial cells, which line all blood vessels.
Johnson formed the CCM1 Consortium in 1995 to coordinate efforts to find the genes involved in this sometimes-devastating condition.