. . . . . . . . . . . . "[Three infants with thiamine-responsive megaloblastic anemia were homozygous, and the parents were heterozygous for a c.196G > T mutation in the SLC19A2 gene on chromosome 1q23.3, which encodes a high-affinity thiamine transporter.]. 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 . "2014-10-02T12:33:16+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .