. . . . . . . "[The mutation detection rate for familial cerebral cavernous malformations (CCM) is extremely high, being about 90�% if direct sequencing of the three genes, CCM1, CCM2, and CCM3, is used in conjunction with quantitative analyses to detect larger CCM1-3 deletions/duplications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:18:07+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .