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Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect.
Nizon, Mathilde; Laugel, Vincent; Flanigan, Kevin M; Pastore, Matthew; Waldrop, Megan A; Rosenfeld, Jill A; Marom, Ronit; Xiao, Rui; Gerard, Amanda; Pichon, Olivier; Le Caignec, Cédric; Gérard, Marion; Dieterich, Klaus; Truitt Cho, Megan; McWalter, Kirsty; Hiatt, Susan; Thompson, Michelle L; Bézieau, Stéphane; Wadley, Alexandrea; Wierenga, Klaas J; Egly, Jean-Marc; Isidor, Bertrand.
Afiliação
  • Nizon M; CHU Nantes, Service de Génétique Médicale, Nantes, France. bertrand.isidor@chu-nantes.fr.
  • Laugel V; L'institut du thorax, INSERM, CNRS, UNIV Nantes, 44007, Nantes, France. bertrand.isidor@chu-nantes.fr.
  • Flanigan KM; Laboratoire de génétique médicale, INSERM UMR 1112, Faculté de Médecine, 11 rue Humann, 67000, Strasbourg, France.
  • Pastore M; Neurology Department, Nationwide Children's Hospital, Columbus, OH, USA.
  • Waldrop MA; Neurology Department, Nationwide Children's Hospital, Columbus, OH, USA.
  • Rosenfeld JA; Neurology Department, Nationwide Children's Hospital, Columbus, OH, USA.
  • Marom R; Baylor College of Medicine, Houston, TX, USA.
  • Xiao R; Baylor College of Medicine, Houston, TX, USA.
  • Gerard A; Baylor College of Medicine, Houston, TX, USA.
  • Pichon O; Baylor College of Medicine, Houston, TX, USA.
  • Le Caignec C; CHU Nantes, Service de Génétique Médicale, Nantes, France.
  • Gérard M; CHU Nantes, Service de Génétique Médicale, Nantes, France.
  • Dieterich K; Service de Génétique Clinique, CHU Caen, Caen, France.
  • Truitt Cho M; Service de Génétique Clinique, CHU Grenoble, Grenoble, France.
  • McWalter K; Clinical Genomics GeneDx, Gaithersburg, MD, USA.
  • Hiatt S; Clinical Genomics GeneDx, Gaithersburg, MD, USA.
  • Thompson ML; HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
  • Bézieau S; HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
  • Wadley A; CHU Nantes, Service de Génétique Médicale, Nantes, France.
  • Wierenga KJ; L'institut du thorax, INSERM, CNRS, UNIV Nantes, 44007, Nantes, France.
  • Egly JM; University of Oklahoma School of Medicine, Oklahoma City, OK, USA.
  • Isidor B; Mayo Clinic Florida, Jacksonville, FL, 32224, USA.
Genet Med ; 21(11): 2663, 2019 11.
Article em En | MEDLINE | ID: mdl-31267042
ABSTRACT
In the Acknowledgements section of the paper the authors neglected to mention that the study was supported by a grant from the National Human Genome Research Institute (NHGRI) UM1HG007301 (S.H., M.L.T.). In addition, the award of MD was associated with the authors Michelle L. Thompson and Susan Hiatt instead of PhD. The PDF and HTML versions of the Article have been modified accordingly.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article