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Published Erratum
. 2019 Jul 1:4:16.
doi: 10.1038/s41525-019-0090-y. eCollection 2019.

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

Anne-Claude Tabet #  1   2   3   4 Thomas Rolland #  2   3   4 Marie Ducloy  2   3   4 Jonathan Lévy  1 Julien Buratti  2   3   4 Alexandre Mathieu  2   3   4 Damien Haye  1 Laurence Perrin  1 Céline Dupont  1 Sandrine Passemard  1 Yline Capri  1 Alain Verloes  1 Séverine Drunat  1 Boris Keren  5 Cyril Mignot  6 Isabelle Marey  7 Aurélia Jacquette  7 Sandra Whalen  7 Eva Pipiras  8 Brigitte Benzacken  8 Sandra Chantot-Bastaraud  9 Alexandra Afenjar  10 Delphine Héron  10 Cédric Le Caignec  11 Claire Beneteau  11 Olivier Pichon  11 Bertrand Isidor  11 Albert David  11 Laila El Khattabi  12 Stephan Kemeny  13 Laetitia Gouas  13 Philippe Vago  13 Anne-Laure Mosca-Boidron  14 Laurence Faivre  15 Chantal Missirian  16 Nicole Philip  16 Damien Sanlaville  17 Patrick Edery  18 Véronique Satre  19 Charles Coutton  19 Françoise Devillard  19 Klaus Dieterich  20 Marie-Laure Vuillaume  21 Caroline Rooryck  21 Didier Lacombe  21 Lucile Pinson  22 Vincent Gatinois  22 Jacques Puechberty  22 Jean Chiesa  23 James Lespinasse  24 Christèle Dubourg  25 Chloé Quelin  25 Mélanie Fradin  25 Hubert Journel  26 Annick Toutain  27 Dominique Martin  28 Abdelamdjid Benmansour  1 Claire S Leblond  2   3   4 Roberto Toro  2   3   4 Frédérique Amsellem  29 Richard Delorme  2   3   4   29 Thomas Bourgeron  2   3   4
Affiliations
Published Erratum

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

Anne-Claude Tabet et al. NPJ Genom Med. .

Abstract

[This corrects the article DOI: 10.1038/s41525-017-0035-2.].

Keywords: Clinical genetics; Neurodevelopmental disorders.

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Erratum for

  • A framework to identify contributing genes in patients with Phelan-McDermid syndrome.
    Tabet AC, Rolland T, Ducloy M, Lévy J, Buratti J, Mathieu A, Haye D, Perrin L, Dupont C, Passemard S, Capri Y, Verloes A, Drunat S, Keren B, Mignot C, Marey I, Jacquette A, Whalen S, Pipiras E, Benzacken B, Chantot-Bastaraud S, Afenjar A, Héron D, Le Caignec C, Beneteau C, Pichon O, Isidor B, David A, El Khattabi L, Kemeny S, Gouas L, Vago P, Mosca-Boidron AL, Faivre L, Missirian C, Philip N, Sanlaville D, Edery P, Satre V, Coutton C, Devillard F, Dieterich K, Vuillaume ML, Rooryck C, Lacombe D, Pinson L, Gatinois V, Puechberty J, Chiesa J, Lespinasse J, Dubourg C, Quelin C, Fradin M, Journel H, Toutain A, Martin D, Benmansour A, Leblond CS, Toro R, Amsellem F, Delorme R, Bourgeron T. Tabet AC, et al. NPJ Genom Med. 2017 Oct 23;2:32. doi: 10.1038/s41525-017-0035-2. eCollection 2017. NPJ Genom Med. 2017. PMID: 29263841 Free PMC article.

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