. . . . . . . "[the first fully characterized gross deletion in the LAMA2 gene, encompassing exon 56 (c.7750-1713 _ 7899-2153del), detected in 31% of congenital muscular dystrophy type 1A patients]. 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 . "2017-10-17T13:14:13+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .