Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect

Mathilde Nizon^{1

2}, Vincent Laugel³, Kevin M Flanigan⁴, Matthew Pastore⁴, Megan A Waldrop⁴, Jill A Rosenfeld⁵, Ronit Marom⁵, Rui Xiao⁵, Amanda Gerard⁵, Olivier Pichon⁶, Cédric Le Caignec⁶, Marion Gérard⁷, Klaus Dieterich⁸, Megan Truitt Cho⁹, Kirsty McWalter⁹, Susan Hiatt¹⁰, Michelle L Thompson¹⁰, Stéphane Bézieau^{6

11}, Alexandrea Wadley¹², Klaas J Wierenga¹³, Jean-Marc Egly¹⁴, Bertrand Isidor^{6

11}

Affiliations

¹ CHU Nantes, Service de Génétique Médicale, Nantes, France. bertrand.isidor@chu-nantes.fr.
² L'institut du thorax, INSERM, CNRS, UNIV Nantes, 44007, Nantes, France. bertrand.isidor@chu-nantes.fr.
³ Laboratoire de génétique médicale, INSERM UMR 1112, Faculté de Médecine, 11 rue Humann, 67000, Strasbourg, France.
⁴ Neurology Department, Nationwide Children's Hospital, Columbus, OH, USA.
⁵ Baylor College of Medicine, Houston, TX, USA.
⁶ CHU Nantes, Service de Génétique Médicale, Nantes, France.
⁷ Service de Génétique Clinique, CHU Caen, Caen, France.
⁸ Service de Génétique Clinique, CHU Grenoble, Grenoble, France.
⁹ Clinical Genomics GeneDx, Gaithersburg, MD, USA.
¹⁰ HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
¹¹ L'institut du thorax, INSERM, CNRS, UNIV Nantes, 44007, Nantes, France.
¹² University of Oklahoma School of Medicine, Oklahoma City, OK, USA.
¹³ Mayo Clinic Florida, Jacksonville, FL, 32224, USA.
¹⁴ Institut de génétique et de biologie moléculaire cellulaire IGBMC, Faculté de Médecine, Strasbourg, France.

PMID: 31267042
DOI: 10.1038/s41436-019-0590-2

Free article

Published Erratum

Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect

Mathilde Nizon et al. Genet Med. 2019 Nov.

Free article

. 2019 Nov;21(11):2663.

doi: 10.1038/s41436-019-0590-2.

Authors

Affiliations

¹ CHU Nantes, Service de Génétique Médicale, Nantes, France. bertrand.isidor@chu-nantes.fr.
² L'institut du thorax, INSERM, CNRS, UNIV Nantes, 44007, Nantes, France. bertrand.isidor@chu-nantes.fr.
³ Laboratoire de génétique médicale, INSERM UMR 1112, Faculté de Médecine, 11 rue Humann, 67000, Strasbourg, France.
⁴ Neurology Department, Nationwide Children's Hospital, Columbus, OH, USA.
⁵ Baylor College of Medicine, Houston, TX, USA.
⁶ CHU Nantes, Service de Génétique Médicale, Nantes, France.
⁷ Service de Génétique Clinique, CHU Caen, Caen, France.
⁸ Service de Génétique Clinique, CHU Grenoble, Grenoble, France.
⁹ Clinical Genomics GeneDx, Gaithersburg, MD, USA.
¹⁰ HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
¹¹ L'institut du thorax, INSERM, CNRS, UNIV Nantes, 44007, Nantes, France.
¹² University of Oklahoma School of Medicine, Oklahoma City, OK, USA.
¹³ Mayo Clinic Florida, Jacksonville, FL, 32224, USA.
¹⁴ Institut de génétique et de biologie moléculaire cellulaire IGBMC, Faculté de Médecine, Strasbourg, France.

PMID: 31267042
DOI: 10.1038/s41436-019-0590-2

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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Erratum for

Variants in MED12L, encoding a subunit of the mediator kinase module, are responsible for intellectual disability associated with transcriptional defect.
Nizon M, Laugel V, Flanigan KM, Pastore M, Waldrop MA, Rosenfeld JA, Marom R, Xiao R, Gerard A, Pichon O, Le Caignec C, Gérard M, Dieterich K, Truitt Cho M, McWalter K, Hiatt S, Thompson ML, Bézieau S, Wadley A, Wierenga KJ, Egly JM, Isidor B. Nizon M, et al. Genet Med. 2019 Dec;21(12):2713-2722. doi: 10.1038/s41436-019-0557-3. Epub 2019 Jun 3. Genet Med. 2019. PMID: 31155615 Free PMC article.

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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

Affiliations

Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect

Authors

Affiliations

Abstract

Erratum for

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