T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency.
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DOI: 10.1182/blood-2018-07-863431
Abstract: ARPC1B is a key factor for the assembly and maintenance of the ARP2/3 complex that is involved in actin branching from an existing filament. Germline biallelic mutations in ARPC1B have been recently described in 6… read more here.
Keywords: defects patients; combined immunodeficiency; patients arpc1b; cell defects ... See more keywords