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Published in 2021 at "Clinical Genetics"
DOI: 10.1111/cge.13975
Abstract: Glanzmann's thrombasthenia (GT) is a severe hemorrhagic disease. It is caused by mutations in ITGA2B or ITGB3, which are the respective genes encoding integrin αIIb and β3. Despite widespread mutational analysis, the mechanisms underlying the…
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Keywords:
bleeding severity;
mice;
2659c q887x;
itga2b 2659c ... See more keywords