[Impaired UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) enzyme function, not lack of expression, may be the key pathogenic factor in hereditary inclusion body myopathy (HIBM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
Gene-disease associations inferred from text-mining the literature.
DisGeNET evidence - LITERATURE