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Updated: Apr 6, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Clinically focused exome sequencing identifies an homozygous mutation that confers DOCK8 deficiency
Allison J Burbank1,2, Shaili N Shah1,2, Maureen Montgomery3
1Departments of Medicine, Division of Rheumatology, Allergy and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
No abstract available in PubMed .
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