. . . . . . . . . . . . "[results indicate that carriage of the homozygous 211 G to A variation within the coding region is an additive risk factor for neonatal hyperbilirubinemia in G6PD-deficient Taiwanese male neonates.]. 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 . "2014-10-02T12:33:21+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .