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Updated: May 23, 2026

From a 2DE-Gel Spot to Protein Function: Lesson Learned From HS1 in Chronic Lymphocytic Leukemia
Published on: October 19, 2014
A compound heterozygous case of leukocyte adhesion deficiency type-1 with moderate CD18 expression and severe disease
Jeremy Richard Brozyna1, Rosemary Moak1, Loretta Modica Parker2
1Division of Allergy and Immunology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA.
Abstract:
A child with severe leukocyte adhesion deficiency type-1 (LAD-1) was found to have compound heterozygous ITGB2 mutations. Despite moderate CD18 expression, the patient experienced life-threatening infections, demonstrating that protein levels do not always correlate with clinical severity.
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