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

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Main Authors: Reivla Marques Vasconcelos Soares, Monique Alvares da Silva, Julliane Tamara Araújo de Melo Campos, Josivan Gomes Lima
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-12-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2024.1508146/full
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author Reivla Marques Vasconcelos Soares
Monique Alvares da Silva
Julliane Tamara Araújo de Melo Campos
Julliane Tamara Araújo de Melo Campos
Josivan Gomes Lima
author_facet Reivla Marques Vasconcelos Soares
Monique Alvares da Silva
Julliane Tamara Araújo de Melo Campos
Julliane Tamara Araújo de Melo Campos
Josivan Gomes Lima
author_sort Reivla Marques Vasconcelos Soares
collection DOAJ
format Article
id doaj-art-a6691d36b1ea416d96ff5b2e9b603cc9
institution Kabale University
issn 1664-2392
language English
publishDate 2024-12-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Endocrinology
spelling doaj-art-a6691d36b1ea416d96ff5b2e9b603cc92024-12-03T07:44:26ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922024-12-011510.3389/fendo.2024.15081461508146Corrigendum: Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic featuresReivla Marques Vasconcelos Soares0Monique Alvares da Silva1Julliane Tamara Araújo de Melo Campos2Julliane Tamara Araújo de Melo Campos3Josivan Gomes Lima4Department of Clinical Medicine, Hospital Universitaírio Onofre Lopes (HUOL), Federal University of Rio Grande do Norte (UFRN), Natal, RN, BrazilMolecular Biology and Genomics Laboratory, Federal University of Rio Grande do Norte (UFRN), Natal, RN, BrazilMolecular Biology and Genomics Laboratory, Federal University of Rio Grande do Norte (UFRN), Natal, RN, BrazilDepartment of Morphology (DMOR), Federal University of Rio Grande do Norte (UFRN), Natal, RN, BrazilDepartment of Clinical Medicine, Hospital Universitaírio Onofre Lopes (HUOL), Federal University of Rio Grande do Norte (UFRN), Natal, RN, Brazilhttps://www.frontiersin.org/articles/10.3389/fendo.2024.1508146/fullPPAR gammaadipose tissuegenetic lipodystrophyinsulin resistancediabetes mellitus
spellingShingle Reivla Marques Vasconcelos Soares
Monique Alvares da Silva
Julliane Tamara Araújo de Melo Campos
Julliane Tamara Araújo de Melo Campos
Josivan Gomes Lima
Corrigendum: Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features
Frontiers in Endocrinology
PPAR gamma
adipose tissue
genetic lipodystrophy
insulin resistance
diabetes mellitus
title Corrigendum: Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features
title_full Corrigendum: Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features
title_fullStr Corrigendum: Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features
title_full_unstemmed Corrigendum: Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features
title_short Corrigendum: Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features
title_sort corrigendum familial partial lipodystrophy resulting from loss of function pparγ pathogenic variants phenotypic clinical and genetic features
topic PPAR gamma
adipose tissue
genetic lipodystrophy
insulin resistance
diabetes mellitus
url https://www.frontiersin.org/articles/10.3389/fendo.2024.1508146/full
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AT moniquealvaresdasilva corrigendumfamilialpartiallipodystrophyresultingfromlossoffunctionppargpathogenicvariantsphenotypicclinicalandgeneticfeatures
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AT jullianetamaraaraujodemelocampos corrigendumfamilialpartiallipodystrophyresultingfromlossoffunctionppargpathogenicvariantsphenotypicclinicalandgeneticfeatures
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