. . . . . . . "[Among the several genes and loci associated with FECD, the strongest association is with an intronic (CTG�CAG)n trinucleotide repeat expansion in the TCF4 gene, which is found in the majority of affected 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 . "2017-10-17T13:16:33+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .