Associated Papers
A scalable approach to resolving variants of uncertain significance.
Tejura M et al.
Biorxiv : the Preprint Server for Biology, 2026
41727046 (PubMed )
Supplement: media-7.xlsx › VarChAMP_data_supp_mat_PP
Two CGD Families with a Hypomorphic Mutation in the Activation Domain of p67phox.
Roos D et al.
Journal of Clinical & Cellular Immunology, 2014
Focus on FOCIS: the continuing diagnostic challenge of autosomal recessive chronic granulomatous disease.
Yu G et al.
Clinical Immunology (orlando, Fla.), 2008
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