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European Journal of Human Genetics logoLink to European Journal of Human Genetics
. 2023 Jan 24;32(1):130. doi: 10.1038/s41431-023-01286-z

Correction: The 2019 and 2021 International workshops on Alport syndrome

Sergio Daga 1,2, Jie Ding 3, Constantinos Deltas 4, Judy Savige 5, Beata S Lipska-Ziętkiewicz 6, Julia Hoefele 7, Frances Flinter 8, Daniel P Gale 9,10, Marina Aksenova 11, Hirofumi Kai 12, Laura Perin 13,14, Moumita Barua 15, Roser Torra 16, Jeff H Miner 17, Laura Massella 18, Danica Galešić Ljubanović 19, Rachel Lennon 20, Andrè B Weinstock 21, Bertrand Knebelmann 22, Agne Cerkauskaite 23,24, Susie Gear 25, Oliver Gross 26, A Neil Turner 27, Margherita Baldassarri 1,2,28, Anna Maria Pinto 28, Alessandra Renieri 1,2,28,
PMCID: PMC10772067  PMID: 36690832

Correction to: European Journal of Human Genetics 10.1038/s41431-022-01075-0, published online 09 March 2022

The following acknowledgement was missing from this article.

This research has been supported (not financially) by “European Reference Network for Rare Kidney Disease, ERKNet”. This ERN is partly co-funded by the European Union within the framework of the Third Health Programme “ERN- 2016 - Framework Partnership Agreement 2017-2021”


Articles from European Journal of Human Genetics are provided here courtesy of Nature Publishing Group

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