. . . . . . . "[The mismatch repair enzyme MSH2, implicated in repeat instability in other triplet repeat diseases, is highly expressed in pluripotent cells and occupies FXN intron 1, and shRNA silencing of�MSH2 impedes repeat expansion, providing a possible molecular explanation for repeat expansion in FRDA.]. 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 . "2017-10-17T13:14:43+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .