Published Erratum
doi: 10.1038/s41436-021-01217-7.
Correction to: Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities
Virginie Carmignac
1
2
, Cyril Mignot
3
4
, Emmanuelle Blanchard
5
6
, Paul Kuentz
7
8
, Marie-Hélène Aubriot-Lorton
9
, Victoria E R Parker
10
, Arthur Sorlin
7
8
11
, Sylvie Fraitag
12
, Jean-Benoît Courcet
7
8
11
, Yannis Duffourd
7
8
, Diana Rodriguez
4
, Rachel G Knox
10
, Satyamaanasa Polubothu
13
14
15
, Anne Boland
16
, Robert Olaso
16
, Marc Delepine
16
, Véronique Darmency
11
, Melissa Riachi
14
15
, Chloé Quelin
17
, Paul Rollier
17
, Louise Goujon
17
, Sarah Grotto
18
, Yline Capri
18
, Marie-Line Jacquemont
19
, Sylvie Odent
17
, Daniel Amram
20
, Martin Chevarin
7
21
, Catherine Vincent-Delorme
22
, Benoît Catteau
23
, Laurent Guibaud
24
, Alexis Arzimanoglou
25
26
, Malika Keddar
27
, Catherine Sarret
28
, Patrick Callier
7
8
27
, Didier Bessis
29
, David Geneviève
30
, Jean-François Deleuze
16
, Christel Thauvin
7
8
31
, Robert K Semple
10
32
, Christophe Philippe
7
, Jean-Baptiste Rivière
7
8
, Veronica A Kinsler
13
14
15
, Laurence Faivre
7
8
33
, Pierre Vabres
7
34
8
Affiliations
Affiliations
- 1 INSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France. virginie.carmignac@chu-dijon.fr.
- 2 MAGEC-Mosaïque Reference Center, Dijon University Hospital, Dijon, France. virginie.carmignac@chu-dijon.fr.
- 3 Neuropaediatrics and Development Pathology Department, Trousseau Hospital, AP-HP, Paris, France.
- 4 Genetics Department and Reference Center for rare causes of Intellectual Disability, Pitié-Salpêtrière hospital, AP-HP, Paris, France.
- 5 Plateforme IBiSA de Microscopie Electronique, Anatomie et cytologie pathologique, Université et CHRU de Tours, Tours, France.
- 6 INSERM U1259 MAVIVH, Université et CHRU de Tours, Tours, France.
- 7 INSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
- 8 Fédération Hospitalo-Universitaire Médecine Translationnelle et Anomalies du Développement (TRANSLAD), Dijon-Burgundy University Hospital, Dijon, France.
- 9 Pathology department, Dijon-Burgundy University Hospital, Dijon, France.
- 10 The University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, Cambridge, UK.
- 11 Pediatrics and Medical Genetics Department, Dijon-Bourgogne University Hospital, Dijon, France.
- 12 Service d'Anatomie et Cytologie Pathologique, Necker-Enfants Malades Hospital, Paris, France.
- 13 Paediatric Dermatology, Great Ormond St Hospital for Children NHS Foundation Trust, London, UK.
- 14 UCL GOS Institute of Child Health, London, UK.
- 15 Mosaicism and Precision Medicine laboratory, Francis Crick Institute, London, UK.
- 16 National Genotyping Center, Genomic Institute, CEA, Evry, France.
- 17 Clinical Genetics department, Rennes University Hospital, Rennes, France.
- 18 Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
- 19 Medical Genetics Unit, CHU La Réunion, Saint-Pierre, France.
- 20 Clinical Genetics Department, Créteil Hospital, Créteil, France.
- 21 Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne University Hospital, Dijon, France.
- 22 Medical Genetic Department, Jeanne de Flandre Hospital, Lille, France.
- 23 Dermatology department, Lille University Hospital, Lille, France.
- 24 Pediatric and Fetal Imaging Department, Hospices Civils de Lyon, Bron, France.
- 25 Department of Paediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, University Hospitals of Lyon (HCL), Lyon, France.
- 26 Brain Dynamics and Cognition (DYCOG) Team, Lyon Neuroscience Research Centre, Lyon, France.
- 27 Cytogenetics Department, Dijon University Hospital, Dijon, France.
- 28 Medical genetics department, Pôle Femme et Enfant, Clermont-Ferrand University Hospital-Hôpital d'Estaing, Clermont-Ferrand, France.
- 29 Dermatology Department, Montpellier University Hospital, Montpellier, France.
- 30 Medical Genetics Department, Montpellier University Hospital, Montpellier, France.
- 31 Centre de Référence Déficiences Intellectuelles de Causes Rares, Hôpital d'Enfants, Dijon, France.
- 32 Center for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
- 33 Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Hôpital d'Enfants, Dijon, France.
- 34 MAGEC-Mosaïque Reference Center, Dijon University Hospital, Dijon, France.
- PMID: 34257424
- PMCID: PMC8414795
- DOI: 10.1038/s41436-021-01217-7
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Published Erratum
Correction to: Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities
Virginie Carmignac et al.
Genet Med.
2021 Aug.
Display options
Format
doi: 10.1038/s41436-021-01217-7.
Authors
Virginie Carmignac
1
2
, Cyril Mignot
3
4
, Emmanuelle Blanchard
5
6
, Paul Kuentz
7
8
, Marie-Hélène Aubriot-Lorton
9
, Victoria E R Parker
10
, Arthur Sorlin
7
8
11
, Sylvie Fraitag
12
, Jean-Benoît Courcet
7
8
11
, Yannis Duffourd
7
8
, Diana Rodriguez
4
, Rachel G Knox
10
, Satyamaanasa Polubothu
13
14
15
, Anne Boland
16
, Robert Olaso
16
, Marc Delepine
16
, Véronique Darmency
11
, Melissa Riachi
14
15
, Chloé Quelin
17
, Paul Rollier
17
, Louise Goujon
17
, Sarah Grotto
18
, Yline Capri
18
, Marie-Line Jacquemont
19
, Sylvie Odent
17
, Daniel Amram
20
, Martin Chevarin
7
21
, Catherine Vincent-Delorme
22
, Benoît Catteau
23
, Laurent Guibaud
24
, Alexis Arzimanoglou
25
26
, Malika Keddar
27
, Catherine Sarret
28
, Patrick Callier
7
8
27
, Didier Bessis
29
, David Geneviève
30
, Jean-François Deleuze
16
, Christel Thauvin
7
8
31
, Robert K Semple
10
32
, Christophe Philippe
7
, Jean-Baptiste Rivière
7
8
, Veronica A Kinsler
13
14
15
, Laurence Faivre
7
8
33
, Pierre Vabres
7
34
8
Affiliations
- 1 INSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France. virginie.carmignac@chu-dijon.fr.
- 2 MAGEC-Mosaïque Reference Center, Dijon University Hospital, Dijon, France. virginie.carmignac@chu-dijon.fr.
- 3 Neuropaediatrics and Development Pathology Department, Trousseau Hospital, AP-HP, Paris, France.
- 4 Genetics Department and Reference Center for rare causes of Intellectual Disability, Pitié-Salpêtrière hospital, AP-HP, Paris, France.
- 5 Plateforme IBiSA de Microscopie Electronique, Anatomie et cytologie pathologique, Université et CHRU de Tours, Tours, France.
- 6 INSERM U1259 MAVIVH, Université et CHRU de Tours, Tours, France.
- 7 INSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
- 8 Fédération Hospitalo-Universitaire Médecine Translationnelle et Anomalies du Développement (TRANSLAD), Dijon-Burgundy University Hospital, Dijon, France.
- 9 Pathology department, Dijon-Burgundy University Hospital, Dijon, France.
- 10 The University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, Cambridge, UK.
- 11 Pediatrics and Medical Genetics Department, Dijon-Bourgogne University Hospital, Dijon, France.
- 12 Service d'Anatomie et Cytologie Pathologique, Necker-Enfants Malades Hospital, Paris, France.
- 13 Paediatric Dermatology, Great Ormond St Hospital for Children NHS Foundation Trust, London, UK.
- 14 UCL GOS Institute of Child Health, London, UK.
- 15 Mosaicism and Precision Medicine laboratory, Francis Crick Institute, London, UK.
- 16 National Genotyping Center, Genomic Institute, CEA, Evry, France.
- 17 Clinical Genetics department, Rennes University Hospital, Rennes, France.
- 18 Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
- 19 Medical Genetics Unit, CHU La Réunion, Saint-Pierre, France.
- 20 Clinical Genetics Department, Créteil Hospital, Créteil, France.
- 21 Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne University Hospital, Dijon, France.
- 22 Medical Genetic Department, Jeanne de Flandre Hospital, Lille, France.
- 23 Dermatology department, Lille University Hospital, Lille, France.
- 24 Pediatric and Fetal Imaging Department, Hospices Civils de Lyon, Bron, France.
- 25 Department of Paediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, University Hospitals of Lyon (HCL), Lyon, France.
- 26 Brain Dynamics and Cognition (DYCOG) Team, Lyon Neuroscience Research Centre, Lyon, France.
- 27 Cytogenetics Department, Dijon University Hospital, Dijon, France.
- 28 Medical genetics department, Pôle Femme et Enfant, Clermont-Ferrand University Hospital-Hôpital d'Estaing, Clermont-Ferrand, France.
- 29 Dermatology Department, Montpellier University Hospital, Montpellier, France.
- 30 Medical Genetics Department, Montpellier University Hospital, Montpellier, France.
- 31 Centre de Référence Déficiences Intellectuelles de Causes Rares, Hôpital d'Enfants, Dijon, France.
- 32 Center for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
- 33 Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Hôpital d'Enfants, Dijon, France.
- 34 MAGEC-Mosaïque Reference Center, Dijon University Hospital, Dijon, France.
- PMID: 34257424
- PMCID: PMC8414795
- DOI: 10.1038/s41436-021-01217-7
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Erratum for
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Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities.Carmignac V, Mignot C, Blanchard E, Kuentz P, Aubriot-Lorton MH, Parker VER, Sorlin A, Fraitag S, Courcet JB, Duffourd Y, Rodriguez D, Knox RG, Polubothu S, Boland A, Olaso R, Delepine M, Darmency V, Riachi M, Quelin C, Rollier P, Goujon L, Grotto S, Capri Y, Jacquemont ML, Odent S, Amram D, Chevarin M, Vincent-Delorme C, Catteau B, Guibaud L, Arzimanoglou A, Keddar M, Sarret C, Callier P, Bessis D, Geneviève D, Deleuze JF, Thauvin C, Semple RK, Philippe C, Rivière JB, Kinsler VA, Faivre L, Vabres P. Carmignac V, et al. Genet Med. 2021 Aug;23(8):1484-1491. doi: 10.1038/s41436-021-01161-6. Epub 2021 Apr 8. Genet Med. 2021. PMID: 33833411 Free PMC article.
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