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Irene Simonetta1*
Renata Riolo1Federica Todaro1
Vincenzo Donadio2
Alex Incensi2Salvatore Miceli1
Paolo Colomba3Giovanni Duro3
Antonino Tuttolomondo1- 1Internal Medicine and Stroke Care Ward, Regional Reference Center for Diagnosis and Treatment of Anderson-Fabry Disease, Department of Health Promotion, Maternal and Child Health, Internal Medicine and Specialty Excellence “G. D’Alessandro” (PROMISE), University of Palermo, Palermo, Italy
- 2Neuromuscular and Neuroimmunology Unit, Bellaria Hospital, IRCCS Institute of Neurological Sciences of Bologna, Bologna, Italy
- 3Institute for Biomedical Research and Innovation (IRIB-CNR), National Research Council of Italy, Palermo, Italy
by Simonetta I, Riolo R, Todaro F, Donadio V, Incensi A, Miceli S, Colomba P, Duro G and Tuttolomondo A (2023). Front. Genet. 14:1122893. doi: 10.3389/fgene.2023.1122893
In the published article, there was an error in the Author list, and authors Salvatore Miceli, Paolo Colomba, Giovanni Duro were erroneously excluded. The corrected Author list appears below.
“Irene Simonetta, Renata Riolo, Federica Todaro, Vincenzo Donadio, Alex Incensi, Salvatore Miceli, Paolo Colomba, Giovanni Duro, Antonino Tuttolomondo.”
In the published article, there was an error in affiliation 1. Instead of “Complex Operating Unit of Internal Medicine with Stroke Care, Regional Reference Center for Diagnosis and Treatment of Anderson-Fabry Disease, Department of Health Promotion, Maternal and Child Health, Internal Medicine and Specialty Excellence “G. D’Alessandro” (PROMISE), University of Palermo, Palermo, Italy”, it should be “Internal Medicine and Stroke Care Ward, Regional Reference Center for Diagnosis and Treatment of Anderson-Fabry Disease, Department of Health Promotion, Maternal and Child Health, Internal Medicine and Specialty Excellence “G. D’Alessandro” (PROMISE), University of Palermo, Palermo, Italy”.
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.
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Keywords: Anderson–Fabry disease, de novo pathogenic variant, one family member, renal disease, case report
Citation: Simonetta I, Riolo R, Todaro F, Donadio V, Incensi A, Miceli S, Colomba P, Duro G and Tuttolomondo A (2024) Corrigendum: Case report: De novo mutation of a-galactosidase A in a female patient with end-stage renal disease: report of a case of late diagnosis of Anderson–Fabry disease. Front. Genet. 15:1368953. doi: 10.3389/fgene.2024.1368953
Received: 11 January 2024; Accepted: 01 February 2024;
Published: 15 February 2024.
Approved by:
Frontiers Editorial Office, Frontiers Media SA, SwitzerlandCopyright © 2024 Simonetta, Riolo, Todaro, Donadio, Incensi, Miceli, Colomba, Duro and Tuttolomondo. 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: Irene Simonetta, aXJlbmUuc2ltb25ldHRhQGxpdmUuaXQ=