Skip to main content

CORRECTION article

Front. Endocrinol., 03 December 2024
Sec. Clinical Diabetes
Volume 15 - 2024 | https://doi.org/10.3389/fendo.2024.1508146

Corrigendum: Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features

This article is a correction to:

  1. Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features

    1. Read original article
Reivla Marques Vasconcelos SoaresReivla Marques Vasconcelos Soares1Monique Alvares da SilvaMonique Alvares da Silva2Julliane Tamara Araújo de Melo Campos,Julliane Tamara Araújo de Melo Campos2,3Josivan Gomes Lima*Josivan Gomes Lima1*
  • 1Department of Clinical Medicine, Hospital Universitaírio Onofre Lopes (HUOL), Federal University of Rio Grande do Norte (UFRN), Natal, RN, Brazil
  • 2Molecular Biology and Genomics Laboratory, Federal University of Rio Grande do Norte (UFRN), Natal, RN, Brazil
  • 3Department of Morphology (DMOR), Federal University of Rio Grande do Norte (UFRN), Natal, RN, Brazil

A Corrigendum on
Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features

By Soares RMV, da Silva MA, Campos JTAdM and Lima JG (2024). Front. Endocrinol. 15:1394102. doi: 10.3389/fendo.2024.1394102

In the published article, there was an error in the Funding statement. The Funding statement was displayed as “The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Finance Code 001”. The correct Funding statement appears below.

“The authors declare that financial support was received for manuscript processing charges and the open access fee from Chiesi Global Rare Diseases (GRD). Chiesi GRD was not involved in the design, data collection, interpretation or decision to publish this manuscript.”

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: PPAR gamma, adipose tissue, genetic lipodystrophy, insulin resistance, diabetes mellitus

Citation: Soares RMV, da Silva MA, Campos JTAdM and Lima JG (2024) Corrigendum: Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features. Front. Endocrinol. 15:1508146. doi: 10.3389/fendo.2024.1508146

Received: 08 October 2024; Accepted: 29 October 2024;
Published: 03 December 2024.

Approved by:

Frontiers Editorial Office, Frontiers Media SA, Switzerland

Copyright © 2024 Soares, da Silva, Campos and Lima. 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: Josivan Gomes Lima, am9zaXZhbmxpbWFAZ21haWwuY29t

Disclaimer: 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.