Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations
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DOI: 10.1016/j.jns.2017.06.043
Abstract: Cerebral cavernous malformations (CCMs) are clusters of capillaries in the brain that may cause focal deficits or seizures in affected patients. They occur in both sporadic and inherited autosomal dominant form. Germline mutations in CCM1,… read more here.
Keywords: ccm; cavernous malformations; cerebral cavernous; gene ... See more keywords