This article is a correction to:
Genetic investigation of Nordic patients with complement-mediated kidney diseases
Viktor Rydberg
Sigridur Sunna Aradottir
Ann-Charlotte Kristoffersson
Diana KarpmanA Corrigendum on
Genetic investigation of Nordic patients with complement-mediated kidney diseases
By Rydberg V, Aradottir SS, Kristoffersson A-C, Svitacheva N and Karpman D (2023). Front. Immunol. 14:1254759. doi: 10.3389/fimmu.2023.1254759
In the published article, there was an error in Table 3 as published. Under the heading C3, rowc.4030-4C>G was under the ACMG classification stated as “P” when it should be “LB”. Under the heading CFHR2, row R141S, “c.423G>A” should have been written as “c.423G>T”. And finally, under the heading CLU, row K444Q, “c.1339A>C” should be corrected to “c.1330A>C”. The corrected Table 3 and its caption appear below.
Table 3
Table 3. Variants in C3G patients included in this study.
In the published article, there was an error in Supplementary Table 1. The C3 level of patient 314 was given as “normal” when it should have been written as “low”. The corrected Supplementary Material File has now been published.
The authors apologize for these errors and state that they do not change the scientific conclusions of the article in any way. The original article has been updated.
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Keywords: complement, atypical hemolytic uremic syndrome, C3 glomerulopathy, membranoproliferative glomerulonephritis, genes
Citation: Rydberg V, Aradottir SS, Kristoffersson A-C, Svitacheva N and Karpman D (2024) Corrigendum: Genetic investigation of Nordic patients with complement-mediated kidney diseases. Front. Immunol. 15:1476204. doi: 10.3389/fimmu.2024.1476204
Received: 05 August 2024; Accepted: 08 August 2024;
Published: 23 August 2024.
Edited and Reviewed by:
Francesca Granucci, University of Milano-Bicocca, ItalyCopyright © 2024 Rydberg, Aradottir, Kristoffersson, Svitacheva and Karpman. 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.
*Correspondence: Diana Karpman, diana.karpman@med.lu.se