. . . . . . . "[We and others have previously reported that heterozygous mutations in PIK3CD encoding the p110? catalytic PI3K subunit cause a unique disorder termed p110?-activating mutations causing senescent T cells, lymphadenopathy, and immunodeficiency (PASLI) disease.]. 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 . "2017-10-17T13:15:23+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .