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. 2022 Mar 17;3:836465. doi: 10.3389/falgy.2022.836465

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Copyright © 2022 Szabó, Csuka, Andrási, Varga, Farkas and Szilágyi.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Family tree of a patient with the novel SERPING1 exon 7 duplication. Affected members of the family are depicted with dark symbols, while all available results of complement and genetic measurements are denoted below the symbols. Def. or normal C1-INH means deficient or normal activity and level of C1-inhibitor, respectively. “Exon 7 dup” refers to the heterozygous carrier state of the duplication of SERPING1 exon 7, while individuals denoted as “exon 7 wild” does not carry this variation.