A novel CCM3 mutation associated with cerebral cavernous malformation in a Chinese family
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DOI: 10.1177/1756286420902664
Abstract: Background: Cerebral cavernous malformation (CCM), especially the familial form, is a relatively rare congenital and occult vascular disease of the central nervous system. The familial form of CCM has been linked to three different genes:… read more here.
Keywords: family; pdcd10 ccm3; ccm3; cerebral cavernous ... See more keywords