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Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome

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Autores principales: Tabet, Anne-Claude, Rolland, Thomas, Ducloy, Marie, Lévy, Jonathan, Buratti, Julien, Mathieu, Alexandre, Haye, Damien, Perrin, Laurence, Dupont, Céline, Passemard, Sandrine, Capri, Yline, Verloes, Alain, Drunat, Séverine, Keren, Boris, Mignot, Cyril, Marey, Isabelle, Jacquette, Aurélia, Whalen, Sandra, Pipiras, Eva, Benzacken, Brigitte, Chantot-Bastaraud, Sandra, Afenjar, Alexandra, Héron, Delphine, Le Caignec, Cédric, Beneteau, Claire, Pichon, Olivier, Isidor, Bertrand, David, Albert, El Khattabi, Laila, Kemeny, Stephan, Gouas, Laetitia, Vago, Philippe, Mosca-Boidron, Anne-Laure, Faivre, Laurence, Missirian, Chantal, Philip, Nicole, Sanlaville, Damien, Edery, Patrick, Satre, Véronique, Coutton, Charles, Devillard, Françoise, Dieterich, Klaus, Vuillaume, Marie-Laure, Rooryck, Caroline, Lacombe, Didier, Pinson, Lucile, Gatinois, Vincent, Puechberty, Jacques, Chiesa, Jean, Lespinasse, James, Dubourg, Christèle, Quelin, Chloé, Fradin, Mélanie, Journel, Hubert, Toutain, Annick, Martin, Dominique, Benmansour, Abdelamdjid, Leblond, Claire S., Toro, Roberto, Amsellem, Frédérique, Delorme, Richard, Bourgeron, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602945/
https://www.ncbi.nlm.nih.gov/pubmed/31285849
http://dx.doi.org/10.1038/s41525-019-0090-y
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author Tabet, Anne-Claude
Rolland, Thomas
Ducloy, Marie
Lévy, Jonathan
Buratti, Julien
Mathieu, Alexandre
Haye, Damien
Perrin, Laurence
Dupont, Céline
Passemard, Sandrine
Capri, Yline
Verloes, Alain
Drunat, Séverine
Keren, Boris
Mignot, Cyril
Marey, Isabelle
Jacquette, Aurélia
Whalen, Sandra
Pipiras, Eva
Benzacken, Brigitte
Chantot-Bastaraud, Sandra
Afenjar, Alexandra
Héron, Delphine
Le Caignec, Cédric
Beneteau, Claire
Pichon, Olivier
Isidor, Bertrand
David, Albert
El Khattabi, Laila
Kemeny, Stephan
Gouas, Laetitia
Vago, Philippe
Mosca-Boidron, Anne-Laure
Faivre, Laurence
Missirian, Chantal
Philip, Nicole
Sanlaville, Damien
Edery, Patrick
Satre, Véronique
Coutton, Charles
Devillard, Françoise
Dieterich, Klaus
Vuillaume, Marie-Laure
Rooryck, Caroline
Lacombe, Didier
Pinson, Lucile
Gatinois, Vincent
Puechberty, Jacques
Chiesa, Jean
Lespinasse, James
Dubourg, Christèle
Quelin, Chloé
Fradin, Mélanie
Journel, Hubert
Toutain, Annick
Martin, Dominique
Benmansour, Abdelamdjid
Leblond, Claire S.
Toro, Roberto
Amsellem, Frédérique
Delorme, Richard
Bourgeron, Thomas
author_facet Tabet, Anne-Claude
Rolland, Thomas
Ducloy, Marie
Lévy, Jonathan
Buratti, Julien
Mathieu, Alexandre
Haye, Damien
Perrin, Laurence
Dupont, Céline
Passemard, Sandrine
Capri, Yline
Verloes, Alain
Drunat, Séverine
Keren, Boris
Mignot, Cyril
Marey, Isabelle
Jacquette, Aurélia
Whalen, Sandra
Pipiras, Eva
Benzacken, Brigitte
Chantot-Bastaraud, Sandra
Afenjar, Alexandra
Héron, Delphine
Le Caignec, Cédric
Beneteau, Claire
Pichon, Olivier
Isidor, Bertrand
David, Albert
El Khattabi, Laila
Kemeny, Stephan
Gouas, Laetitia
Vago, Philippe
Mosca-Boidron, Anne-Laure
Faivre, Laurence
Missirian, Chantal
Philip, Nicole
Sanlaville, Damien
Edery, Patrick
Satre, Véronique
Coutton, Charles
Devillard, Françoise
Dieterich, Klaus
Vuillaume, Marie-Laure
Rooryck, Caroline
Lacombe, Didier
Pinson, Lucile
Gatinois, Vincent
Puechberty, Jacques
Chiesa, Jean
Lespinasse, James
Dubourg, Christèle
Quelin, Chloé
Fradin, Mélanie
Journel, Hubert
Toutain, Annick
Martin, Dominique
Benmansour, Abdelamdjid
Leblond, Claire S.
Toro, Roberto
Amsellem, Frédérique
Delorme, Richard
Bourgeron, Thomas
author_sort Tabet, Anne-Claude
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spelling pubmed-66029452019-07-08 Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome Tabet, Anne-Claude Rolland, Thomas Ducloy, Marie Lévy, Jonathan Buratti, Julien Mathieu, Alexandre Haye, Damien Perrin, Laurence Dupont, Céline Passemard, Sandrine Capri, Yline Verloes, Alain Drunat, Séverine Keren, Boris Mignot, Cyril Marey, Isabelle Jacquette, Aurélia Whalen, Sandra Pipiras, Eva Benzacken, Brigitte Chantot-Bastaraud, Sandra Afenjar, Alexandra Héron, Delphine Le Caignec, Cédric Beneteau, Claire Pichon, Olivier Isidor, Bertrand David, Albert El Khattabi, Laila Kemeny, Stephan Gouas, Laetitia Vago, Philippe Mosca-Boidron, Anne-Laure Faivre, Laurence Missirian, Chantal Philip, Nicole Sanlaville, Damien Edery, Patrick Satre, Véronique Coutton, Charles Devillard, Françoise Dieterich, Klaus Vuillaume, Marie-Laure Rooryck, Caroline Lacombe, Didier Pinson, Lucile Gatinois, Vincent Puechberty, Jacques Chiesa, Jean Lespinasse, James Dubourg, Christèle Quelin, Chloé Fradin, Mélanie Journel, Hubert Toutain, Annick Martin, Dominique Benmansour, Abdelamdjid Leblond, Claire S. Toro, Roberto Amsellem, Frédérique Delorme, Richard Bourgeron, Thomas NPJ Genom Med Author Correction Nature Publishing Group UK 2019-07-01 /pmc/articles/PMC6602945/ /pubmed/31285849 http://dx.doi.org/10.1038/s41525-019-0090-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Author Correction
Tabet, Anne-Claude
Rolland, Thomas
Ducloy, Marie
Lévy, Jonathan
Buratti, Julien
Mathieu, Alexandre
Haye, Damien
Perrin, Laurence
Dupont, Céline
Passemard, Sandrine
Capri, Yline
Verloes, Alain
Drunat, Séverine
Keren, Boris
Mignot, Cyril
Marey, Isabelle
Jacquette, Aurélia
Whalen, Sandra
Pipiras, Eva
Benzacken, Brigitte
Chantot-Bastaraud, Sandra
Afenjar, Alexandra
Héron, Delphine
Le Caignec, Cédric
Beneteau, Claire
Pichon, Olivier
Isidor, Bertrand
David, Albert
El Khattabi, Laila
Kemeny, Stephan
Gouas, Laetitia
Vago, Philippe
Mosca-Boidron, Anne-Laure
Faivre, Laurence
Missirian, Chantal
Philip, Nicole
Sanlaville, Damien
Edery, Patrick
Satre, Véronique
Coutton, Charles
Devillard, Françoise
Dieterich, Klaus
Vuillaume, Marie-Laure
Rooryck, Caroline
Lacombe, Didier
Pinson, Lucile
Gatinois, Vincent
Puechberty, Jacques
Chiesa, Jean
Lespinasse, James
Dubourg, Christèle
Quelin, Chloé
Fradin, Mélanie
Journel, Hubert
Toutain, Annick
Martin, Dominique
Benmansour, Abdelamdjid
Leblond, Claire S.
Toro, Roberto
Amsellem, Frédérique
Delorme, Richard
Bourgeron, Thomas
Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome
title Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome
title_full Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome
title_fullStr Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome
title_full_unstemmed Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome
title_short Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome
title_sort author correction: a framework to identify contributing genes in patients with phelan-mcdermid syndrome
topic Author Correction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602945/
https://www.ncbi.nlm.nih.gov/pubmed/31285849
http://dx.doi.org/10.1038/s41525-019-0090-y
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