UNVEILING A LESS SEVERE CONGENITAL NEPHROTIC SYNDROME IN A RAPA NUI PATIENT WITH A NPHS1 MAORI FOUNDER VARIANT
- 1Instituto de Medicina, Facultad de Medicina, Universidad Austral de Chile, Valdivia, Chile
- 2Departamento de Pediatría y Cirugía Infantil Oriente, Facultad de Medicina, Universidad de Chile, Santiago de Chile, Chile
- 3Unidad de Nefrología, Diálisis y Trasplante Renal, Hospital Luis Calvo Mackenna, Santiago de Chile, Chile
- 4Unidad de Lactantes, Hospital Luis Calvo Mackenna, Santiago de Chile, Chile
- 5Programa de Telesalud, Hospital Luis Calvo Mackenna, Santiago de Chile, Chile
A Corrigendum on
Case report: Unveiling a less severe congenital nephrotic syndrome in a Rapa Nui patient with a NPHS1 Maori founder variant
by Krall P, Rojo A, Plaza A, Canals S, Ceballos ML, Cano F and Guerrero JL (2024). Front. Nephrol. 4:1379061. doi: 10.3389/fneph.2024.1379061
In the published article, there was an error in the Funding statement. The funding statement for the article was displayed with the recognition of FONDECYT #111-40242. The correct statement is FONDECYT #111-40242 and INGE 210028 from the Vicerrectoría de Investigación y Desarrollo, Universidad de Chile. The correct Funding statement appears below.
Funding
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The genetic analysis was funded by the FONDECYT #111-40242. The publication of this article was funded by INGE 210028 from the Vicerrectoría de Investigación y Desarrollo, Universidad de Chile.
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.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Keywords: congenital nephrotic syndrome, NPHS1, kidney survival, Maori founder variant, Rapa Nui (Easter Island)
Citation: Krall P, Rojo A, Plaza A, Canals S, Ceballos ML, Cano F and Guerrero JL (2024) Corrigendum: Case report: Unveiling a less severe congenital nephrotic syndrome in a Rapa Nui patient with a NPHS1 Maori founder variant. Front. Nephrol. 4:1454138. doi: 10.3389/fneph.2024.1454138
Received: 24 June 2024; Accepted: 25 June 2024;
Published: 03 July 2024.
Approved by:
Frontiers Editorial Office, Frontiers Media SA, SwitzerlandCopyright © 2024 Krall, Rojo, Plaza, Canals, Ceballos, Cano and Guerrero. 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: Paola Krall, paola.krall@uchile.cl