Figure 1.
(A) IRF2BP2 c. 1652G>A segregated only in family members diagnosed with CVID. (B) The resulting p.S551N mutation occurs in the RING domain of IRF2BP2 (denoted by the arrow).
(A) IRF2BP2 c. 1652G>A segregated only in family members diagnosed with CVID. (B) The resulting p.S551N mutation occurs in the RING domain of IRF2BP2 (denoted by the arrow).