. . . . . . . . . . . . "[We describe for the first time a homozygous HFE splice site mutation (IVS5 G/A) in a non-Caucasian patient with hereditary hemochromatosis. Although the absence of this novel HFE gene mutation in Caucasian subjects suggests that the mutation is exclusive ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2015-02-21"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2016-05-13T12:42:21+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .