. . . . . . . "[2 new homozygous mutations in introns 6 & 7 represent the first Bbeta-chain splicing mutations in afibrinogenemia/+ 13C > T creates a donor splice site in intron 6/+ 1G > T removes the invariant GT of intron 7 donor splice site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:12:41+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .