. . . . . . . "[One of the two brothers with a more severe phenotype coinherited also had G6PD deficiency, while both had microcytosis due to the homozygosity for the non-deletional form of ?-thalassemia ATG?ACG substitution at the initiation codon of the alpha2 globin gene.]. 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 . "2017-10-17T13:19:07+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .