Analysis of 14 Patients With Congenital Nephrotic Syndrome
A Corrigendum on
Analysis of 14 Patients With Congenital Nephrotic Syndrome
by Chen, Y., Zhang, Y., Wang, F., Zhang, H., Zhong, X., Xiao, H., et al. (2019). Front. Pediatr. 7:341. doi: 10.3389/fped.2019.00341
In the original article, there was a mistake in Table 3 as published. In No. 13, the NPHS1 mutation “c.1135C>T, p. Ala379Thr” was incorrect and should be “c.1135C>T, p. Arg379Trp.” Furthermore, in case No. 6, the NPHS1 mutation “c.1339G>A, p. Glu477Lys” should be “c.1339G>A, p. Glu447Lys.” The corrected Table 3 appears below.
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
Keywords: congenital nephrotic syndrome, genetic defect, cytomegalovirus infection, clinical manifestation, prognosis
Citation: Chen Y, Zhang Y, Wang F, Zhang H, Zhong X, Xiao H, Yao Y, Jiang Y, Ding J and Hou X (2019) Corrigendum: Analysis of 14 Patients With Congenital Nephrotic Syndrome. Front. Pediatr. 7:471. doi: 10.3389/fped.2019.00471
Received: 17 September 2019; Accepted: 28 October 2019;
Published: 13 November 2019.
Edited by:
Jakub Zieg, University Hospital in Motol, CzechiaReviewed by:
Dagmara Borzych-Duzalka, Medical University of Gdansk, PolandCopyright © 2019 Chen, Zhang, Wang, Zhang, Zhong, Xiao, Yao, Jiang, Ding and Hou. 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: Xinlin Hou, qian.d@husky.neu.edu