Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria(European Journal of Human Genetics, (2021), 29, 8, (1186-1197), 10.1038/s41431-021-00858-1)

Judy Savige; Helen Storey; Elizabeth Watson; Jens Michael Hertz; Constantinos Deltas; Alessandra Renieri; Francesca Mari; Pascale Hilbert; Pavlina Plevova; Peter Byers; Agne Cerkauskaite; Martin Gregory; Rimante Cerkauskiene; Danica Galesic Ljubanovic; Francesca Becherucci; Carmela Errichiello; Laura Massella; Valeria Aiello; Rachel Lennon; Louise Hopkinson; Ania Koziell; Adrian Lungu; Hansjorg Martin Rothe; Julia Hoefele; Miriam Zacchia; Tamara Nikuseva Martic; Asheeta Gupta; Albertien van Eerde; Susie Gear; Samuela Landini; Viviana Palazzo; Laith al-Rabadi; Kathleen Claes; Anniek Corveleyn; Evelien Van Hoof; Micheel van Geel; Maggie Williams; Emma Ashton; Hendica Belge; Elisabeth Ars; Agnieszka Bierzynska; Concetta Gangemi; Beata S. Lipska-Ziętkiewicz

doi:10.1038/s41431-023-01288-x

Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria(European Journal of Human Genetics, (2021), 29, 8, (1186-1197), 10.1038/s41431-021-00858-1)

Judy Savige^*, Helen Storey, Elizabeth Watson, Jens Michael Hertz, Constantinos Deltas, Alessandra Renieri, Francesca Mari, Pascale Hilbert, Pavlina Plevova, Peter Byers, Agne Cerkauskaite, Martin Gregory, Rimante Cerkauskiene, Danica Galesic Ljubanovic, Francesca Becherucci, Carmela Errichiello, Laura Massella, Valeria Aiello, Rachel Lennon, Louise HopkinsonAnia Koziell, Adrian Lungu, Hansjorg Martin Rothe, Julia Hoefele, Miriam Zacchia, Tamara Nikuseva Martic, Asheeta Gupta, Albertien van Eerde, Susie Gear, Samuela Landini, Viviana Palazzo, Laith al-Rabadi, Kathleen Claes, Anniek Corveleyn, Evelien Van Hoof, Micheel van Geel, Maggie Williams, Emma Ashton, Hendica Belge, Elisabeth Ars, Agnieszka Bierzynska, Concetta Gangemi, Beata S. Lipska-Ziętkiewicz

^*Corresponding author for this work

Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

1 Downloads (Pure)

Abstract

Correction to: European Journal of Human Genetics (2021) 29:1186–1197 The following Acknowledgement was missing: 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”. The original article has been corrected.

Original language	English
Article number	132
Number of pages	1
Journal	European Journal of Human Genetics
Volume	32
Issue number	1
Early online date	2023
DOIs	https://doi.org/10.1038/s41431-023-01288-x
Publication status	Published - Jan 2024

Access to Document

10.1038/s41431-023-01288-xLicence: CC BY

s41431-023-01288-xFinal published version, 482 KBLicence: CC BY

Fingerprint

Dive into the research topics of 'Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria(European Journal of Human Genetics, (2021), 29, 8, (1186-1197), 10.1038/s41431-021-00858-1)'. Together they form a unique fingerprint.

Cite this

Savige, J., Storey, H., Watson, E., Hertz, J. M., Deltas, C., Renieri, A., Mari, F., Hilbert, P., Plevova, P., Byers, P., Cerkauskaite, A., Gregory, M., Cerkauskiene, R., Ljubanovic, D. G., Becherucci, F., Errichiello, C., Massella, L., Aiello, V., Lennon, R., ... Lipska-Ziętkiewicz, B. S. (2024). Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria(European Journal of Human Genetics, (2021), 29, 8, (1186-1197), 10.1038/s41431-021-00858-1). European Journal of Human Genetics, 32(1), Article 132. https://doi.org/10.1038/s41431-023-01288-x

@article{0f03c6d8c5fc432fa3166ba7a944c71c,

title = "Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria(European Journal of Human Genetics, (2021), 29, 8, (1186-1197), 10.1038/s41431-021-00858-1)",

abstract = "Correction to: European Journal of Human Genetics (2021) 29:1186–1197 The following Acknowledgement was missing: 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”. The original article has been corrected.",

author = "Judy Savige and Helen Storey and Elizabeth Watson and Hertz, {Jens Michael} and Constantinos Deltas and Alessandra Renieri and Francesca Mari and Pascale Hilbert and Pavlina Plevova and Peter Byers and Agne Cerkauskaite and Martin Gregory and Rimante Cerkauskiene and Ljubanovic, {Danica Galesic} and Francesca Becherucci and Carmela Errichiello and Laura Massella and Valeria Aiello and Rachel Lennon and Louise Hopkinson and Ania Koziell and Adrian Lungu and Rothe, {Hansjorg Martin} and Julia Hoefele and Miriam Zacchia and Martic, {Tamara Nikuseva} and Asheeta Gupta and {van Eerde}, Albertien and Susie Gear and Samuela Landini and Viviana Palazzo and Laith al-Rabadi and Kathleen Claes and Anniek Corveleyn and {Van Hoof}, Evelien and {van Geel}, Micheel and Maggie Williams and Emma Ashton and Hendica Belge and Elisabeth Ars and Agnieszka Bierzynska and Concetta Gangemi and Lipska-Zi{\c e}tkiewicz, {Beata S.}",

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

year = "2024",

month = jan,

doi = "10.1038/s41431-023-01288-x",

language = "English",

volume = "32",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Nature Publishing Group",

number = "1",

}

Savige, J, Storey, H, Watson, E, Hertz, JM, Deltas, C, Renieri, A, Mari, F, Hilbert, P, Plevova, P, Byers, P, Cerkauskaite, A, Gregory, M, Cerkauskiene, R, Ljubanovic, DG, Becherucci, F, Errichiello, C, Massella, L, Aiello, V, Lennon, R, Hopkinson, L, Koziell, A, Lungu, A, Rothe, HM, Hoefele, J, Zacchia, M, Martic, TN, Gupta, A, van Eerde, A, Gear, S, Landini, S, Palazzo, V, al-Rabadi, L, Claes, K, Corveleyn, A, Van Hoof, E, van Geel, M, Williams, M, Ashton, E, Belge, H, Ars, E, Bierzynska, A, Gangemi, C & Lipska-Ziętkiewicz, BS 2024, 'Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria(European Journal of Human Genetics, (2021), 29, 8, (1186-1197), 10.1038/s41431-021-00858-1)', European Journal of Human Genetics, vol. 32, no. 1, 132. https://doi.org/10.1038/s41431-023-01288-x

Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria(European Journal of Human Genetics, (2021), 29, 8, (1186-1197), 10.1038/s41431-021-00858-1). / Savige, Judy; Storey, Helen; Watson, Elizabeth et al.
In: European Journal of Human Genetics, Vol. 32, No. 1, 132, 01.2024.

Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

TY - JOUR

T1 - Correction

T2 - Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria(European Journal of Human Genetics, (2021), 29, 8, (1186-1197), 10.1038/s41431-021-00858-1)

AU - Savige, Judy

AU - Storey, Helen

AU - Watson, Elizabeth

AU - Hertz, Jens Michael

AU - Deltas, Constantinos

AU - Renieri, Alessandra

AU - Mari, Francesca

AU - Hilbert, Pascale

AU - Plevova, Pavlina

AU - Byers, Peter

AU - Cerkauskaite, Agne

AU - Gregory, Martin

AU - Cerkauskiene, Rimante

AU - Ljubanovic, Danica Galesic

AU - Becherucci, Francesca

AU - Errichiello, Carmela

AU - Massella, Laura

AU - Aiello, Valeria

AU - Lennon, Rachel

AU - Hopkinson, Louise

AU - Koziell, Ania

AU - Lungu, Adrian

AU - Rothe, Hansjorg Martin

AU - Hoefele, Julia

AU - Zacchia, Miriam

AU - Martic, Tamara Nikuseva

AU - Gupta, Asheeta

AU - van Eerde, Albertien

AU - Gear, Susie

AU - Landini, Samuela

AU - Palazzo, Viviana

AU - al-Rabadi, Laith

AU - Claes, Kathleen

AU - Corveleyn, Anniek

AU - Van Hoof, Evelien

AU - van Geel, Micheel

AU - Williams, Maggie

AU - Ashton, Emma

AU - Belge, Hendica

AU - Ars, Elisabeth

AU - Bierzynska, Agnieszka

AU - Gangemi, Concetta

AU - Lipska-Ziętkiewicz, Beata S.

N1 - Funding Information: 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”. Publisher Copyright: © 2023 The Author(s).

PY - 2024/1

Y1 - 2024/1

N2 - Correction to: European Journal of Human Genetics (2021) 29:1186–1197 The following Acknowledgement was missing: 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”. The original article has been corrected.

AB - Correction to: European Journal of Human Genetics (2021) 29:1186–1197 The following Acknowledgement was missing: 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”. The original article has been corrected.

UR - http://www.scopus.com/inward/record.url?scp=85147128342&partnerID=8YFLogxK

U2 - 10.1038/s41431-023-01288-x

DO - 10.1038/s41431-023-01288-x

M3 - Comment/Letter to the editor

C2 - 36721056

AN - SCOPUS:85147128342

SN - 1018-4813

VL - 32

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 1

M1 - 132

ER -

Savige J, Storey H, Watson E, Hertz JM, Deltas C, Renieri A et al. Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria(European Journal of Human Genetics, (2021), 29, 8, (1186-1197), 10.1038/s41431-021-00858-1). European Journal of Human Genetics. 2024 Jan;32(1):132. Epub 2023. doi: 10.1038/s41431-023-01288-x

Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria(European Journal of Human Genetics, (2021), 29, 8, (1186-1197), 10.1038/s41431-021-00858-1)

Abstract

Access to Document

Other files and links

Fingerprint

Cite this