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 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

Research output: Contribution to journal › Comment/debate › peer-review

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
Pages (from-to)	132
Number of pages	1
Journal	European Journal of Human Genetics
Volume	32
Issue number	1
DOIs	https://doi.org/10.1038/s41431-023-01288-x
Publication status	Published - Jan 2024
Externally published	Yes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

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10.1038/s41431-023-01288-x

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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.

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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), 132. https://doi.org/10.1038/s41431-023-01288-x

@article{0ea1199ae69844d4a28b93102ad0d51c,

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

year = "2024",

month = jan,

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

language = "English",

volume = "32",

pages = "132",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Springer Nature",

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, pp. 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, 01.2024, p. 132.

Research output: Contribution to journal › Comment/debate › 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.

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 - https://www.scopus.com/pages/publications/85147128342

U2 - 10.1038/s41431-023-01288-x

DO - 10.1038/s41431-023-01288-x

M3 - Comment/debate

C2 - 36721056

AN - SCOPUS:85147128342

SN - 1018-4813

VL - 32

SP - 132

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 1

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. 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

UN SDGs

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