. . . . . . . "[Heterozygotes for the mutant Fbn1 allele mg?loxPneo, carrying the same internal deletion of exons 19-24 as the mg? mouse model, present defective microfibrillar deposition, emphysema, deterioration of aortic wall and kyphosis.]. 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 . "2017-10-17T13:12:39+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .