[105 of 150 type 1 von Willebrand disease patients had mutations identified/subgroup with abnormal multimers (57 of 150) had a high prevalence of VWF gene mutations (54 of 57)/with qualitatively normal VWF had fewer mutation (51 of 93).]. 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