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ARPC1B
NM_005720.4:p.A212_V226del15
Associated Papers
Molecular analysis and immunological characterization of a founder mutation causing ARPC1B deficiency.
Dobrose MM et al.
Genes and Immunity, 2025
Recurrent eosinophilia with a novel homozygous ARPC1B mutation.
Sonmez G et al.
Frontiers of Medicine, 2025
Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait?
Chiriaco M et al.
Frontiers in Immunology, 2022
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