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

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Title: Erratum: Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome.
Authors: Tabet AC; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France.; 2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.; 3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France.; 4Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Université Paris Diderot, Paris, France., Rolland T; 2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.; 3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France.; 4Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Université Paris Diderot, Paris, France., Ducloy M; 2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.; 3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France.; 4Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Université Paris Diderot, Paris, France., Lévy J; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France., Buratti J; 2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.; 3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France.; 4Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Université Paris Diderot, Paris, France., Mathieu A; 2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.; 3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France.; 4Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Université Paris Diderot, Paris, France., Haye D; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France., Perrin L; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France., Dupont C; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France., Passemard S; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France., Capri Y; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France., Verloes A; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France., Drunat S; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France., Keren B; 5Cytogenetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France., Mignot C; 6Neurogenetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France., Marey I; 7Clinical Genetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France., Jacquette A; 7Clinical Genetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France., Whalen S; 7Clinical Genetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France., Pipiras E; 8Cytogenetics Unit, Jean Verdier Hospital, APHP, Bondy, France., Benzacken B; 8Cytogenetics Unit, Jean Verdier Hospital, APHP, Bondy, France., Chantot-Bastaraud S; 9Cytogenetics Unit, Trousseau Hospital, APHP, Paris, France., Afenjar A; 10Clinical Genetics Unit, Trousseau Hospital, APHP, Paris, France., Héron D; 10Clinical Genetics Unit, Trousseau Hospital, APHP, Paris, France., Le Caignec C; 11Clinical Genetics Unit, Nantes Hospital, Nantes, France., Beneteau C; 11Clinical Genetics Unit, Nantes Hospital, Nantes, France., Pichon O; 11Clinical Genetics Unit, Nantes Hospital, Nantes, France., Isidor B; 11Clinical Genetics Unit, Nantes Hospital, Nantes, France., David A; 11Clinical Genetics Unit, Nantes Hospital, Nantes, France., El Khattabi L; 12Cytogenetics Unit, Cochin Hospital, APHP, Paris, France., Kemeny S; 13Genetics Unit, CHU Estaing, Clermont-Ferrand, France., Gouas L; 13Genetics Unit, CHU Estaing, Clermont-Ferrand, France., Vago P; 13Genetics Unit, CHU Estaing, Clermont-Ferrand, France., Mosca-Boidron AL; Cytogenetics Unit, Dijon Hospital, Dijon, France., Faivre L; Clinical Genetics Unit, Dijon Hospital, Dijon, France., Missirian C; 16Genetics Unit, La Timone Hospital, Marseille, France., Philip N; 16Genetics Unit, La Timone Hospital, Marseille, France., Sanlaville D; Cytogenetics Unit, Lyon Civil Hospital, Lyon, France., Edery P; Clinical Genetics Unit, Lyon Civil Hospital, Lyon, France., Satre V; 19Cytogenetics Unit, Grenoble Hospital, Grenoble, France., Coutton C; 19Cytogenetics Unit, Grenoble Hospital, Grenoble, France., Devillard F; 19Cytogenetics Unit, Grenoble Hospital, Grenoble, France., Dieterich K; 20Clinical Genetics Unit, Grenoble Hospital, Grenoble, France., Vuillaume ML; 21Genetics Unit, Bordeaux Hospital, Bordeaux, France., Rooryck C; 21Genetics Unit, Bordeaux Hospital, Bordeaux, France., Lacombe D; 21Genetics Unit, Bordeaux Hospital, Bordeaux, France., Pinson L; 22Genetics Unit, Montpellier Hospital, Montpellier, France., Gatinois V; 22Genetics Unit, Montpellier Hospital, Montpellier, France., Puechberty J; 22Genetics Unit, Montpellier Hospital, Montpellier, France., Chiesa J; Genetics Unit, CHRU Nimes, Nimes, France., Lespinasse J; Cytogenetics Unit, Chambéry-Hôtel-Dieu Hospital, Chambéry, France., Dubourg C; 25Genetics Unit, CHU Rennes, Rennes, France., Quelin C; 25Genetics Unit, CHU Rennes, Rennes, France., Fradin M; 25Genetics Unit, CHU Rennes, Rennes, France., Journel H; Genetics Unit, Chubert Hospital, Vannes, France., Toutain A; 27Genetics Unit, Bretonneau Hospital, Tours, France., Martin D; 28Genetics Unit, CH Le Mans, Le Mans, France., Benmansour A; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France., Leblond CS; 2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.; 3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France.; 4Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Université Paris Diderot, Paris, France., Toro R; 2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.; 3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France.; 4Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Université Paris Diderot, Paris, France., Amsellem F; 29Department of Child and Adolescent Psychiatry, Robert Debré Hospital, APHP, Paris, France., Delorme R; 2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.; 3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France.; 4Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Université Paris Diderot, Paris, France.; 29Department of Child and Adolescent Psychiatry, Robert Debré Hospital, APHP, Paris, France., Bourgeron T; 2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.; 3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France.; 4Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Université Paris Diderot, Paris, France.
Source: NPJ genomic medicine [NPJ Genom Med] 2019 Jul 01; Vol. 4, pp. 16. Date of Electronic Publication: 2019 Jul 01 (Print Publication: 2019).
Publication Type: Journal Article; Published Erratum
Journal Info: Publisher: Springer Nature in partnership with the Center of Excellence in Genomic Medicine Research at King Abdulaziz University Country of Publication: England NLM ID: 101685193 Publication Model: eCollection Cited Medium: Internet ISSN: 2056-7944 (Electronic) Linking ISSN: 20567944 NLM ISO Abbreviation: NPJ Genom Med Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: Erratum: Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome.
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            NameFull: Edery P
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            NameFull: Satre V
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          Name:
            NameFull: Coutton C
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          Name:
            NameFull: Devillard F
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          Name:
            NameFull: Dieterich K
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          Name:
            NameFull: Vuillaume ML
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          Name:
            NameFull: Rooryck C
      – PersonEntity:
          Name:
            NameFull: Lacombe D
      – PersonEntity:
          Name:
            NameFull: Pinson L
      – PersonEntity:
          Name:
            NameFull: Gatinois V
      – PersonEntity:
          Name:
            NameFull: Puechberty J
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          Name:
            NameFull: Chiesa J
      – PersonEntity:
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            NameFull: Lespinasse J
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            NameFull: Dubourg C
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            NameFull: Quelin C
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            NameFull: Fradin M
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            NameFull: Journel H
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            NameFull: Toutain A
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          Name:
            NameFull: Martin D
      – PersonEntity:
          Name:
            NameFull: Benmansour A
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          Name:
            NameFull: Leblond CS
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          Name:
            NameFull: Toro R
      – PersonEntity:
          Name:
            NameFull: Amsellem F
      – PersonEntity:
          Name:
            NameFull: Delorme R
      – PersonEntity:
          Name:
            NameFull: Bourgeron T
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 07
              Text: 2019 Jul 01
              Type: published
              Y: 2019
          Identifiers:
            – Type: issn-electronic
              Value: 2056-7944
          Numbering:
            – Type: volume
              Value: 4
          Titles:
            – TitleFull: NPJ genomic medicine
              Type: main
ResultId 1