. . . . . . . . . . . . "[Lattice phenotype resulting from TGFBI A546D mutation in this family is distinct from that observed in previously described pedigree carrying the A546D mutation and exhibiting phenotype designated ' polymorphic corneal amyloidosis '.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2015-08-25T14:39:38+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .