. . . . . . . "[Considering the phenotypic overlap of ADA2 deficiency with the type I interferonopathy Aicardi-Gouti�res syndrome due to mutations in SAMHD1, we looked for the presence of an interferon signature in the peripheral blood of two newly ascertained ADA2-deficient patients.]. 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 . "2017-10-17T13:18:18+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .