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Published in 2017 at "Blood"
DOI: 10.1182/blood.v130.suppl_1.4821.4821
Abstract: LAD-I is a rare disorder of leukocyte adhesion, resulting from ITGB2 gene mutations encoding for the Beta-2 Integrin component CD18. CD18 deficiencies prevent integrin dimerization and endothelial leukocyte adhesion, essential for extravasation and antimicrobial activity.…
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Keywords:
lad;
cd18;
hsct;
leukocyte adhesion ... See more keywords