Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect (Genetics in Medicine, (2019), 10.1038/s41436-019-0557-3)

Mathilde Nizon; Vincent Laugel; Kevin M. Flanigan; Matthew Pastore; Megan A. Waldrop; Jill A. Rosenfeld; Ronit Marom; Rui Xiao; Amanda Gerard; Olivier Pichon; Cédric Le Caignec; Marion Gérard; Klaus Dieterich; Megan Truitt Cho; Kirsty McWalter; Susan Hiatt; Michelle L. Thompson; Stéphane Bézieau; Alexandrea Wadley; Klaas J. Wierenga; Jean Marc Egly; Bertrand Isidor

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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 (Genetics in Medicine, (2019), 10.1038/s41436-019-0557-3)

Genetics in Medicine

DOI: 10.1038/s41436-019-0590-2

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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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Nizon, M., Laugel, V., Flanigan, K. M., Pastore, M., Waldrop, M. A., Rosenfeld, J. A., … Isidor, B. (2019, November 1). Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect (Genetics in Medicine, (2019), 10.1038/s41436-019-0557-3). Genetics in Medicine. Nature Publishing Group. https://doi.org/10.1038/s41436-019-0590-2

Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect (Genetics in Medicine, (2019), 10.1038/s41436-019-0557-3)

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