. . . . . . . "[A novel 282\uFFFDkb duplication (????(282)) was identified in family A and a novel 235\uFFFDkb deletion (--(235)) in family B. Proband A is a coinheritance of ?(CD41-42) and ????(282) and showed severe ?-thalassemia intermedia phenotype.]. 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 . "2017-10-17T13:14:01+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .