Correction to: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study (European Journal of Human Genetics, (2024), 10.1038/s41431-024-01560-8)

Alix Paulet; Cavan Bennett-Ness; Faustine Ageorges; Detlef Trost; Andrew Green; David Goudie; Rosalyn Jewell; Minna Kraatari-Tiri; Juliette PIARD; Christine Coubes; Wayne Lam; Sally Ann Lynch; Samuel Groeschel; Francis Ramond; Joël Fluss; Christina Fagerberg; Charlotte Brasch Andersen; Konstantinos Varvagiannis; Tjitske Kleefstra; Bénédicte Gérard; Mélanie Fradin; Antonio Vitobello; Romano Tenconi; Anne Sophie Denommé-Pichon; Aline Vincent-Devulder; Tobias Haack; Joseph A. Marsh; Lone Walentin Laulund; Mona Grimmel; Angelika Riess; Elke de Boer; Sergio Padilla-Lopez; Somayeh Bakhtiari; Adam Ostendorf; Christiane Zweier; Thomas Smol; Marjolaine Willems; Laurence Faivre; Marcello Scala; Pasquale Striano; Irene Bagnasco; Daniel Koboldt; Maria Iascone; Manon Suerink; Michael C. Kruer; Jonathan Levy; Alain Verloes; Catherine M. Abbott; Lyse Ruaud

doi:10.1038/s41431-024-01606-x

Correction to: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study (European Journal of Human Genetics, (2024), 10.1038/s41431-024-01560-8)

Alix Paulet, Cavan Bennett-Ness, Faustine Ageorges, Detlef Trost, Andrew Green, David Goudie, Rosalyn Jewell, Minna Kraatari-Tiri, Juliette PIARD, Christine Coubes, Wayne Lam, Sally Ann Lynch, Samuel Groeschel, Francis Ramond, Joël Fluss, Christina Fagerberg, Charlotte Brasch Andersen, Konstantinos Varvagiannis, Tjitske Kleefstra, Bénédicte GérardMélanie Fradin, Antonio Vitobello, Romano Tenconi, Anne Sophie Denommé-Pichon, Aline Vincent-Devulder, Tobias Haack, Joseph A. Marsh, Lone Walentin Laulund, Mona Grimmel, Angelika Riess, Elke de Boer, Sergio Padilla-Lopez, Somayeh Bakhtiari, Adam Ostendorf, Christiane Zweier, Thomas Smol, Marjolaine Willems, Laurence Faivre, Marcello Scala, Pasquale Striano, Irene Bagnasco, Daniel Koboldt, Maria Iascone, Manon Suerink, Michael C. Kruer, Jonathan Levy, Alain Verloes, Catherine M. Abbott, Lyse Ruaud

Pediatrics

Research output: Contribution to journal › Comment/debate

Abstract

Correction to: European Journal of Human Geneticshttps://doi.org/10.1038/s41431-024-01560-8, published online 15 February 2024 In the original version of this article, the given and family names of Samuel Groeschel were incorrectly structured. The name was displayed correctly in all versions at the time of publication. The authors, Adam Ostendorf, Christiane Zweier, Thomas Smol, Marjolaine Willems, Laurence Faivre, Marcello Scala, Pasquale Striano, Irene Bagnasco, Daniel Koboldt, Maria Iascone, Manon Suerink were missing from the author list. Moreover, the author contribution texts have been updated in accordance with addition of authors. The original article has been corrected.

Original language	English
Journal	European Journal of Human Genetics
DOIs	https://doi.org/10.1038/s41431-024-01606-x
State	Accepted/In press - 2024

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Paulet, A., Bennett-Ness, C., Ageorges, F., Trost, D., Green, A., Goudie, D., Jewell, R., Kraatari-Tiri, M., PIARD, J., Coubes, C., Lam, W., Lynch, S. A., Groeschel, S., Ramond, F., Fluss, J., Fagerberg, C., Brasch Andersen, C., Varvagiannis, K., Kleefstra, T., ... Ruaud, L. (Accepted/In press). Correction to: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study (European Journal of Human Genetics, (2024), 10.1038/s41431-024-01560-8). European Journal of Human Genetics. https://doi.org/10.1038/s41431-024-01606-x

@article{a61c3c9d65844d85b2786540edba0848,

title = "Correction to: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study (European Journal of Human Genetics, (2024), 10.1038/s41431-024-01560-8)",

abstract = "Correction to: European Journal of Human Geneticshttps://doi.org/10.1038/s41431-024-01560-8, published online 15 February 2024 In the original version of this article, the given and family names of Samuel Groeschel were incorrectly structured. The name was displayed correctly in all versions at the time of publication. The authors, Adam Ostendorf, Christiane Zweier, Thomas Smol, Marjolaine Willems, Laurence Faivre, Marcello Scala, Pasquale Striano, Irene Bagnasco, Daniel Koboldt, Maria Iascone, Manon Suerink were missing from the author list. Moreover, the author contribution texts have been updated in accordance with addition of authors. The original article has been corrected.",

author = "Alix Paulet and Cavan Bennett-Ness and Faustine Ageorges and Detlef Trost and Andrew Green and David Goudie and Rosalyn Jewell and Minna Kraatari-Tiri and Juliette PIARD and Christine Coubes and Wayne Lam and Lynch, {Sally Ann} and Samuel Groeschel and Francis Ramond and Jo{\"e}l Fluss and Christina Fagerberg and {Brasch Andersen}, Charlotte and Konstantinos Varvagiannis and Tjitske Kleefstra and B{\'e}n{\'e}dicte G{\'e}rard and M{\'e}lanie Fradin and Antonio Vitobello and Romano Tenconi and Denomm{\'e}-Pichon, {Anne Sophie} and Aline Vincent-Devulder and Tobias Haack and Marsh, {Joseph A.} and Laulund, {Lone Walentin} and Mona Grimmel and Angelika Riess and {de Boer}, Elke and Sergio Padilla-Lopez and Somayeh Bakhtiari and Adam Ostendorf and Christiane Zweier and Thomas Smol and Marjolaine Willems and Laurence Faivre and Marcello Scala and Pasquale Striano and Irene Bagnasco and Daniel Koboldt and Maria Iascone and Manon Suerink and Kruer, {Michael C.} and Jonathan Levy and Alain Verloes and Abbott, {Catherine M.} and Lyse Ruaud",

note = "Publisher Copyright: {\textcopyright} The Author(s), under exclusive licence to European Society of Human Genetics 2024.",

year = "2024",

doi = "10.1038/s41431-024-01606-x",

language = "English",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

}

Paulet, A, Bennett-Ness, C, Ageorges, F, Trost, D, Green, A, Goudie, D, Jewell, R, Kraatari-Tiri, M, PIARD, J, Coubes, C, Lam, W, Lynch, SA, Groeschel, S, Ramond, F, Fluss, J, Fagerberg, C, Brasch Andersen, C, Varvagiannis, K, Kleefstra, T, Gérard, B, Fradin, M, Vitobello, A, Tenconi, R, Denommé-Pichon, AS, Vincent-Devulder, A, Haack, T, Marsh, JA, Laulund, LW, Grimmel, M, Riess, A, de Boer, E, Padilla-Lopez, S, Bakhtiari, S, Ostendorf, A, Zweier, C, Smol, T, Willems, M, Faivre, L, Scala, M, Striano, P, Bagnasco, I, Koboldt, D, Iascone, M, Suerink, M, Kruer, MC, Levy, J, Verloes, A, Abbott, CM & Ruaud, L 2024, 'Correction to: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study (European Journal of Human Genetics, (2024), 10.1038/s41431-024-01560-8)', European Journal of Human Genetics. https://doi.org/10.1038/s41431-024-01606-x

TY - JOUR

T1 - Correction to

T2 - Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study (European Journal of Human Genetics, (2024), 10.1038/s41431-024-01560-8)

AU - Paulet, Alix

AU - Bennett-Ness, Cavan

AU - Ageorges, Faustine

AU - Trost, Detlef

AU - Green, Andrew

AU - Goudie, David

AU - Jewell, Rosalyn

AU - Kraatari-Tiri, Minna

AU - PIARD, Juliette

AU - Coubes, Christine

AU - Lam, Wayne

AU - Lynch, Sally Ann

AU - Groeschel, Samuel

AU - Ramond, Francis

AU - Fluss, Joël

AU - Fagerberg, Christina

AU - Brasch Andersen, Charlotte

AU - Varvagiannis, Konstantinos

AU - Kleefstra, Tjitske

AU - Gérard, Bénédicte

AU - Fradin, Mélanie

AU - Vitobello, Antonio

AU - Tenconi, Romano

AU - Denommé-Pichon, Anne Sophie

AU - Vincent-Devulder, Aline

AU - Haack, Tobias

AU - Marsh, Joseph A.

AU - Laulund, Lone Walentin

AU - Grimmel, Mona

AU - Riess, Angelika

AU - de Boer, Elke

AU - Padilla-Lopez, Sergio

AU - Bakhtiari, Somayeh

AU - Ostendorf, Adam

AU - Zweier, Christiane

AU - Smol, Thomas

AU - Willems, Marjolaine

AU - Faivre, Laurence

AU - Scala, Marcello

AU - Striano, Pasquale

AU - Bagnasco, Irene

AU - Koboldt, Daniel

AU - Iascone, Maria

AU - Suerink, Manon

AU - Kruer, Michael C.

AU - Levy, Jonathan

AU - Verloes, Alain

AU - Abbott, Catherine M.

AU - Ruaud, Lyse

PY - 2024

Y1 - 2024

N2 - Correction to: European Journal of Human Geneticshttps://doi.org/10.1038/s41431-024-01560-8, published online 15 February 2024 In the original version of this article, the given and family names of Samuel Groeschel were incorrectly structured. The name was displayed correctly in all versions at the time of publication. The authors, Adam Ostendorf, Christiane Zweier, Thomas Smol, Marjolaine Willems, Laurence Faivre, Marcello Scala, Pasquale Striano, Irene Bagnasco, Daniel Koboldt, Maria Iascone, Manon Suerink were missing from the author list. Moreover, the author contribution texts have been updated in accordance with addition of authors. The original article has been corrected.

AB - Correction to: European Journal of Human Geneticshttps://doi.org/10.1038/s41431-024-01560-8, published online 15 February 2024 In the original version of this article, the given and family names of Samuel Groeschel were incorrectly structured. The name was displayed correctly in all versions at the time of publication. The authors, Adam Ostendorf, Christiane Zweier, Thomas Smol, Marjolaine Willems, Laurence Faivre, Marcello Scala, Pasquale Striano, Irene Bagnasco, Daniel Koboldt, Maria Iascone, Manon Suerink were missing from the author list. Moreover, the author contribution texts have been updated in accordance with addition of authors. The original article has been corrected.

UR - http://www.scopus.com/inward/record.url?scp=85189303200&partnerID=8YFLogxK

U2 - 10.1038/s41431-024-01606-x

DO - 10.1038/s41431-024-01606-x

M3 - Comment/debate

AN - SCOPUS:85189303200

SN - 1018-4813

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

ER -

Correction to: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study (European Journal of Human Genetics, (2024), 10.1038/s41431-024-01560-8)

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