. . . . . . . "[We examined 21 patients with ?-thalassemia (?-thal) in order to identify some genetic modifying factors: ?-thalassemia mutations, HBG2:g.-158C>T polymorphism, ?-globin gene deletions and (AT)xNz(AT)y motif within the hypersensitive site 2-locus control region (HS2-LCR).]. 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 . "2017-10-17T13:13:12+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .