. . . . . . . "[Homozygous EXOSC3 mutation c.92G?C, p.G31A is a founder mutation causing severe pontocerebellar hypoplasia type 1 among the Czech Roma.]. 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 . "2017-10-17T13:18:29+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .