Correction: The 2019 and 2021 International workshops on Alport syndrome (European Journal of Human Genetics, (2022), 30, 5, (507-516), 10.1038/s41431-022-01075-0)

Sergio Daga; Jie Ding; Constantinos Deltas; Judy Savige; Beata S. Lipska-Ziętkiewicz; Julia Hoefele; Frances Flinter; Daniel P. Gale; Marina Aksenova; Hirofumi Kai; Laura Perin; Moumita Barua; Roser Torra; Jeff H. Miner; Laura Massella; Danica Galešić Ljubanović; Rachel Lennon; Andrè B. Weinstock; Bertrand Knebelmann; Agne Cerkauskaite; Susie Gear; Oliver Gross; A. Neil Turner; Margherita Baldassarri; Anna Maria Pinto; Alessandra Renieri

doi:10.1038/s41431-023-01286-z

Correction: The 2019 and 2021 International workshops on Alport syndrome (European Journal of Human Genetics, (2022), 30, 5, (507-516), 10.1038/s41431-022-01075-0)

Sergio Daga, Jie Ding, Constantinos Deltas, Judy Savige, Beata S. Lipska-Ziętkiewicz, Julia Hoefele, Frances Flinter, Daniel P. Gale, Marina Aksenova, Hirofumi Kai, Laura Perin, Moumita Barua, Roser Torra, Jeff H. Miner, Laura Massella, Danica Galešić Ljubanović, Rachel Lennon, Andrè B. Weinstock, Bertrand Knebelmann, Agne CerkauskaiteSusie Gear, Oliver Gross, A. Neil Turner, Margherita Baldassarri, Anna Maria Pinto, Alessandra Renieri

Research output: Contribution to journal › Comment/debate

Abstract

Correction to: European Journal of Human Genetics, 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”.

Original language	English
Pages (from-to)	130
Number of pages	1
Journal	European Journal of Human Genetics
Volume	32
Issue number	1
DOIs	https://doi.org/10.1038/s41431-023-01286-z
State	Published - Jan 2024

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Daga, S., Ding, J., Deltas, C., Savige, J., Lipska-Ziętkiewicz, B. S., Hoefele, J., Flinter, F., Gale, D. P., Aksenova, M., Kai, H., Perin, L., Barua, M., Torra, R., Miner, J. H., Massella, L., Ljubanović, D. G., Lennon, R., Weinstock, A. B., Knebelmann, B., ... Renieri, A. (2024). Correction: The 2019 and 2021 International workshops on Alport syndrome (European Journal of Human Genetics, (2022), 30, 5, (507-516), 10.1038/s41431-022-01075-0). European Journal of Human Genetics, 32(1), 130. https://doi.org/10.1038/s41431-023-01286-z

@article{2756a7fda97a412198c261fcd9004720,

title = "Correction: The 2019 and 2021 International workshops on Alport syndrome (European Journal of Human Genetics, (2022), 30, 5, (507-516), 10.1038/s41431-022-01075-0)",

abstract = "Correction to: European Journal of Human Genetics, 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”.",

author = "Sergio Daga and Jie Ding and Constantinos Deltas and Judy Savige and Lipska-Zi{\c e}tkiewicz, {Beata S.} and Julia Hoefele and Frances Flinter and Gale, {Daniel P.} and Marina Aksenova and Hirofumi Kai and Laura Perin and Moumita Barua and Roser Torra and Miner, {Jeff H.} and Laura Massella and Ljubanovi{\'c}, {Danica Gale{\v s}i{\'c}} and Rachel Lennon and Weinstock, {Andr{\`e} B.} and Bertrand Knebelmann and Agne Cerkauskaite and Susie Gear and Oliver Gross and Turner, {A. Neil} and Margherita Baldassarri and Pinto, {Anna Maria} and Alessandra Renieri",

note = "Publisher Copyright: {\textcopyright} 2023, The Author(s).",

year = "2024",

month = jan,

doi = "10.1038/s41431-023-01286-z",

language = "English",

volume = "32",

pages = "130",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

number = "1",

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Daga, S, Ding, J, Deltas, C, Savige, J, Lipska-Ziętkiewicz, BS, Hoefele, J, Flinter, F, Gale, DP, Aksenova, M, Kai, H, Perin, L, Barua, M, Torra, R, Miner, JH, Massella, L, Ljubanović, DG, Lennon, R, Weinstock, AB, Knebelmann, B, Cerkauskaite, A, Gear, S, Gross, O, Turner, AN, Baldassarri, M, Pinto, AM & Renieri, A 2024, 'Correction: The 2019 and 2021 International workshops on Alport syndrome (European Journal of Human Genetics, (2022), 30, 5, (507-516), 10.1038/s41431-022-01075-0)', European Journal of Human Genetics, vol. 32, no. 1, pp. 130. https://doi.org/10.1038/s41431-023-01286-z

TY - JOUR

T1 - Correction

T2 - The 2019 and 2021 International workshops on Alport syndrome (European Journal of Human Genetics, (2022), 30, 5, (507-516), 10.1038/s41431-022-01075-0)

AU - Daga, Sergio

AU - Ding, Jie

AU - Deltas, Constantinos

AU - Savige, Judy

AU - Lipska-Ziętkiewicz, Beata S.

AU - Hoefele, Julia

AU - Flinter, Frances

AU - Gale, Daniel P.

AU - Aksenova, Marina

AU - Kai, Hirofumi

AU - Perin, Laura

AU - Barua, Moumita

AU - Torra, Roser

AU - Miner, Jeff H.

AU - Massella, Laura

AU - Ljubanović, Danica Galešić

AU - Lennon, Rachel

AU - Weinstock, Andrè B.

AU - Knebelmann, Bertrand

AU - Cerkauskaite, Agne

AU - Gear, Susie

AU - Gross, Oliver

AU - Turner, A. Neil

AU - Baldassarri, Margherita

AU - Pinto, Anna Maria

AU - Renieri, Alessandra

PY - 2024/1

Y1 - 2024/1

N2 - Correction to: European Journal of Human Genetics, 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”.

AB - Correction to: European Journal of Human Genetics, 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”.

UR - http://www.scopus.com/inward/record.url?scp=85159392156&partnerID=8YFLogxK

U2 - 10.1038/s41431-023-01286-z

DO - 10.1038/s41431-023-01286-z

M3 - Comment/debate

C2 - 36690832

AN - SCOPUS:85159392156

SN - 1018-4813

VL - 32

SP - 130

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 1

ER -

Correction: The 2019 and 2021 International workshops on Alport syndrome (European Journal of Human Genetics, (2022), 30, 5, (507-516), 10.1038/s41431-022-01075-0)

Abstract

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