. . . . . . . "[Findings indicated that the 951-953 (delC) deletion mutation in the FOXL2 gene in the two patients resulted in truncated proteins and hence led to their blepharophimosis, ptosis, and epicanthus inversus syndrome.]. 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 . "2017-10-17T13:10:58+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .