. . . . . . . "[Here, we have analyzed the coding regions of GNAI1, GNAI2, and GNAI3 in a set of young sporadic somatotropinoma patients (n?=?32; mean age of diagnosis 32 years) and familial index cases (n?=?14), thus in patients with a disease phenotype similar to that observed in AIP mutation carriers.]. 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 . "2017-10-17T13:17:39+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .