Published Erratum
doi: 10.1038/s41431-024-01606-x.
Correction: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study
Alix Paulet
1
, Cavan Bennett-Ness
2
, Faustine Ageorges
3
, Detlef Trost
4
, Andrew Green
5
, David Goudie
6
, Rosalyn Jewell
7
, Minna Kraatari-Tiri
8
9
, Juliette Piard
10
, Christine Coubes
11
, Wayne Lam
12
, Sally Ann Lynch
13
, Samuel Groeschel
14
, Francis Ramond
15
, Joël Fluss
16
, Christina Fagerberg
17
, Charlotte Brasch Andersen
18
, Konstantinos Varvagiannis
19
, Tjitske Kleefstra
20
21
22
23
, Bénédicte Gérard
24
, Mélanie Fradin
25
, Antonio Vitobello
26
, Romano Tenconi
27
, Anne-Sophie Denommé-Pichon
28
29
, Aline Vincent-Devulder
30
, Tobias Haack
31
, Joseph A Marsh
32
, Lone Walentin Laulund
33
, Mona Grimmel
31
, Angelika Riess
31
, Elke de Boer
20
21
22
, Sergio Padilla-Lopez
34
, Somayeh Bakhtiari
34
, Adam Ostendorf
35
36
, Christiane Zweier
37
38
, Thomas Smol
39
, Marjolaine Willems
40
41
, Laurence Faivre
42
43
, Marcello Scala
44
45
, Pasquale Striano
44
45
, Irene Bagnasco
46
, Daniel Koboldt
35
, Maria Iascone
47
, Manon Suerink
48
, Michael C Kruer
34
, Jonathan Levy
3
, Alain Verloes
3
, Catherine M Abbott
2
, Lyse Ruaud
3
Affiliations
Affiliations
- 1 Département de Génétique, Hôpital Robert-Debré, Paris, France. alix.paulet@hotmail.fr.
- 2 Centre for Genomic and Experimental Medicine and Simons Initiative for the Developing Brain, Institute of Genetics and Cancer, Edinburgh, Scotland, UK.
- 3 Département de Génétique, Hôpital Robert-Debré, Paris, France.
- 4 Laboratoire Cerba, Saint-Ouen l'Aumône, France.
- 5 UCD School of Medicine and Medical Science Consultant in Clinical Genetics, Dublin, Ireland.
- 6 Regional Genetics Service, NHS Tayside, Dundee, Scotland, UK.
- 7 Yorkshire Regional Genetics Service, Leeds Teaching Hospitals NHS Trust, Leeds, England, UK.
- 8 Department of Clinical Genetics, Research unit of Clinical Medicine, Medical Research Center Oulu, Oulu, Finland.
- 9 Oulu University Hospital and University of Oulu, Oulu, Finland.
- 10 Centre de Génétique Humaine, CHU Besançon, Besançon, France.
- 11 Service de Génétique Médicale, CHU de Montpellier, Montpellier, France.
- 12 South-East of Scotland Clinical Genetics Service, General Hospital, Edinburgh, Scotland, UK.
- 13 Clinical Genetics, Children's Health Ireland, Dublin, Ireland.
- 14 Department of Neuropediatrics, University Children's Hospital, Tuebingen, Germany.
- 15 Service de Génétique, CHU Saint-Etienne - Hôpital Nord, Saint-Etienne, France.
- 16 University Hospitals of Geneva, Geneva, Switzerland.
- 17 Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.
- 18 Human Genetik, Syddansk Universitet, Odense, Denmark.
- 19 Service de Médecine Génétique, Hôpitaux universitaires de Genève, Geneva, Switzerland.
- 20 Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
- 21 Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
- 22 Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.
- 23 Center of Excellence for Neuropsychiatry, Vincent van Gogh Institute for Psychiatry, Venray, The Netherlands.
- 24 Molecular Biology, Nouvel Hôpital Civil, Strasbourg, France.
- 25 Service de Génétique Médicale, Hôpital Sud, CHU de Rennes, Rennes, France.
- 26 UMR-Inserm, Génétique des Anomalies du développement, Université de Bourgogne Franche-Comté, Dijon, France.
- 27 Servizio di Genetica Medica, Dipartimento di Pediatra, Padova, Italia.
- 28 Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.
- 29 UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.
- 30 Génétique Médicale, CHU de Caen, Caen, France.
- 31 Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
- 32 MRC Human Genetics Unit, Western General Hospital, University of Edinburgh, Edinburgh, Scotland, UK.
- 33 H C Andersen Children's Hospital, Odense University Hospital, Odense, Denmark.
- 34 Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
- 35 Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children's Hospital, Colombus, OH, USA.
- 36 Department of Pediatrics, The Ohio State University College of Medicine, Colombus, OH, USA.
- 37 Department of Human Genetics, Inselspital Bern, University of Bern, 3010, Bern, Switzerland.
- 38 Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054, Erlangen, Germany.
- 39 University of Lille, EA7364-RADEME, Medical Genetics Institute, Chu Lille, Lille, France.
- 40 Medical Genetic Department for Rare Diseases and Personalized Medicine, Reference Center AD SOOR, AnDDI-RARE, Groupe DI, Inserm U1298, INM, Montpellier University, Montpellier, France.
- 41 Centre Hospitalier Universitaire de Montpellier, Montpellier, France.
- 42 UMR1231 GAD, Inserm, Université de Bourgogne-Franche Comté, Dijon, France.
- 43 Centre de Référence Maladies Rares « Anomalies du développement et syndromes malformatifs », Centre de Génétique, FHU-TRANSLAD et Institut GIMI, CHU dijon, Bourgogne, Dijon, France.
- 44 Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
- 45 Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.
- 46 Division of Child Neuropsychiatry, Martini Hospital, Torino, Italy.
- 47 Laboratorio Di Genetica Medica, Bergamo, Italy.
- 48 Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
- PMID: 38565641
- PMCID: PMC11369287
- DOI: 10.1038/s41431-024-01606-x
Item in Clipboard
Published Erratum
Correction: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study
Alix Paulet et al.
Eur J Hum Genet.
2024 Sep.
Display options
Format
doi: 10.1038/s41431-024-01606-x.
Authors
Alix Paulet
1
, Cavan Bennett-Ness
2
, Faustine Ageorges
3
, Detlef Trost
4
, Andrew Green
5
, David Goudie
6
, Rosalyn Jewell
7
, Minna Kraatari-Tiri
8
9
, Juliette Piard
10
, Christine Coubes
11
, Wayne Lam
12
, Sally Ann Lynch
13
, Samuel Groeschel
14
, Francis Ramond
15
, Joël Fluss
16
, Christina Fagerberg
17
, Charlotte Brasch Andersen
18
, Konstantinos Varvagiannis
19
, Tjitske Kleefstra
20
21
22
23
, Bénédicte Gérard
24
, Mélanie Fradin
25
, Antonio Vitobello
26
, Romano Tenconi
27
, Anne-Sophie Denommé-Pichon
28
29
, Aline Vincent-Devulder
30
, Tobias Haack
31
, Joseph A Marsh
32
, Lone Walentin Laulund
33
, Mona Grimmel
31
, Angelika Riess
31
, Elke de Boer
20
21
22
, Sergio Padilla-Lopez
34
, Somayeh Bakhtiari
34
, Adam Ostendorf
35
36
, Christiane Zweier
37
38
, Thomas Smol
39
, Marjolaine Willems
40
41
, Laurence Faivre
42
43
, Marcello Scala
44
45
, Pasquale Striano
44
45
, Irene Bagnasco
46
, Daniel Koboldt
35
, Maria Iascone
47
, Manon Suerink
48
, Michael C Kruer
34
, Jonathan Levy
3
, Alain Verloes
3
, Catherine M Abbott
2
, Lyse Ruaud
3
Affiliations
- 1 Département de Génétique, Hôpital Robert-Debré, Paris, France. alix.paulet@hotmail.fr.
- 2 Centre for Genomic and Experimental Medicine and Simons Initiative for the Developing Brain, Institute of Genetics and Cancer, Edinburgh, Scotland, UK.
- 3 Département de Génétique, Hôpital Robert-Debré, Paris, France.
- 4 Laboratoire Cerba, Saint-Ouen l'Aumône, France.
- 5 UCD School of Medicine and Medical Science Consultant in Clinical Genetics, Dublin, Ireland.
- 6 Regional Genetics Service, NHS Tayside, Dundee, Scotland, UK.
- 7 Yorkshire Regional Genetics Service, Leeds Teaching Hospitals NHS Trust, Leeds, England, UK.
- 8 Department of Clinical Genetics, Research unit of Clinical Medicine, Medical Research Center Oulu, Oulu, Finland.
- 9 Oulu University Hospital and University of Oulu, Oulu, Finland.
- 10 Centre de Génétique Humaine, CHU Besançon, Besançon, France.
- 11 Service de Génétique Médicale, CHU de Montpellier, Montpellier, France.
- 12 South-East of Scotland Clinical Genetics Service, General Hospital, Edinburgh, Scotland, UK.
- 13 Clinical Genetics, Children's Health Ireland, Dublin, Ireland.
- 14 Department of Neuropediatrics, University Children's Hospital, Tuebingen, Germany.
- 15 Service de Génétique, CHU Saint-Etienne - Hôpital Nord, Saint-Etienne, France.
- 16 University Hospitals of Geneva, Geneva, Switzerland.
- 17 Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.
- 18 Human Genetik, Syddansk Universitet, Odense, Denmark.
- 19 Service de Médecine Génétique, Hôpitaux universitaires de Genève, Geneva, Switzerland.
- 20 Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
- 21 Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
- 22 Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.
- 23 Center of Excellence for Neuropsychiatry, Vincent van Gogh Institute for Psychiatry, Venray, The Netherlands.
- 24 Molecular Biology, Nouvel Hôpital Civil, Strasbourg, France.
- 25 Service de Génétique Médicale, Hôpital Sud, CHU de Rennes, Rennes, France.
- 26 UMR-Inserm, Génétique des Anomalies du développement, Université de Bourgogne Franche-Comté, Dijon, France.
- 27 Servizio di Genetica Medica, Dipartimento di Pediatra, Padova, Italia.
- 28 Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.
- 29 UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.
- 30 Génétique Médicale, CHU de Caen, Caen, France.
- 31 Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
- 32 MRC Human Genetics Unit, Western General Hospital, University of Edinburgh, Edinburgh, Scotland, UK.
- 33 H C Andersen Children's Hospital, Odense University Hospital, Odense, Denmark.
- 34 Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
- 35 Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children's Hospital, Colombus, OH, USA.
- 36 Department of Pediatrics, The Ohio State University College of Medicine, Colombus, OH, USA.
- 37 Department of Human Genetics, Inselspital Bern, University of Bern, 3010, Bern, Switzerland.
- 38 Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054, Erlangen, Germany.
- 39 University of Lille, EA7364-RADEME, Medical Genetics Institute, Chu Lille, Lille, France.
- 40 Medical Genetic Department for Rare Diseases and Personalized Medicine, Reference Center AD SOOR, AnDDI-RARE, Groupe DI, Inserm U1298, INM, Montpellier University, Montpellier, France.
- 41 Centre Hospitalier Universitaire de Montpellier, Montpellier, France.
- 42 UMR1231 GAD, Inserm, Université de Bourgogne-Franche Comté, Dijon, France.
- 43 Centre de Référence Maladies Rares « Anomalies du développement et syndromes malformatifs », Centre de Génétique, FHU-TRANSLAD et Institut GIMI, CHU dijon, Bourgogne, Dijon, France.
- 44 Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
- 45 Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.
- 46 Division of Child Neuropsychiatry, Martini Hospital, Torino, Italy.
- 47 Laboratorio Di Genetica Medica, Bergamo, Italy.
- 48 Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
- PMID: 38565641
- PMCID: PMC11369287
- DOI: 10.1038/s41431-024-01606-x
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Erratum for
-
Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study.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. Paulet A, et al. Eur J Hum Genet. 2024 Sep;32(9):1144-1149. doi: 10.1038/s41431-024-01560-8. Epub 2024 Feb 15. Eur J Hum Genet. 2024. PMID: 38355961 Free PMC article.
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