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Updated: Oct 27, 2026

00:06
In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
DOCK2 deficiency due to a novel cryptic splice site mutation
Manisha Ahuja1,2, Ina C D Schim van der Loeff1,3, Helen Griffin1
1Translational and Clinical Research Institute, Newcastle University , Newcastle upon Tyne, UK.
Abstract:
Autosomal recessive dedicator of cytokinesis 2 (DOCK2) deficiency causes severe, early-onset bacterial and viral infections. We report three siblings with DOCK2 deficiency due to a novel homozygous synonymous variant that results in cryptic mRNA splicing and absence of wild-type protein.
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