. . . . . . . "[Congenital muscular dystrophies (CMD) with hypoglycosylation of ?-dystroglycan are clinically and genetically heterogeneous disorders that are often associated with brain malformations and eye defects.]. 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 . "2017-10-17T13:11:56+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .