Matches in Nanopublications for { ?s ?p "[We report the largest international study on Glanzmann thrombasthenia (GT), an inherited bleeding disorder where defects of the ITGA2B and ITGB3 genes cause quantitative or qualitative defects of the ?IIb?3 integrin, a key mediator of platelet aggregation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1267323.RAQ1hProcVC0ivxPl1YnBgQnTKwf1ZpQiHI6D2UGn3mjo130_assertion description "[We report the largest international study on Glanzmann thrombasthenia (GT), an inherited bleeding disorder where defects of the ITGA2B and ITGB3 genes cause quantitative or qualitative defects of the ?IIb?3 integrin, a key mediator of platelet aggregation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267323.RAQ1hProcVC0ivxPl1YnBgQnTKwf1ZpQiHI6D2UGn3mjo130_provenance.
- NP1267324.RAkLdDDwjHNI3gpjRxj3iAPzgHDhg0mNnvejzfuRUKQuc130_assertion description "[We report the largest international study on Glanzmann thrombasthenia (GT), an inherited bleeding disorder where defects of the ITGA2B and ITGB3 genes cause quantitative or qualitative defects of the ?IIb?3 integrin, a key mediator of platelet aggregation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267324.RAkLdDDwjHNI3gpjRxj3iAPzgHDhg0mNnvejzfuRUKQuc130_provenance.