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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

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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https://hal-normandie-univ.archives-ouvertes.fr/hal-02268423
Contributeur : Marion Gerard <>
Soumis le : mardi 20 août 2019 - 21:50:54
Dernière modification le : jeudi 23 avril 2020 - 14:26:27

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Mathilde Nizon, Vincent Laugel, Kevin M Flanigan, Matthew Pastore, Megan A. Waldrop, et al.. Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect. Genetics in Medicine, Nature Publishing Group, 2019, ⟨10.1038/s41436-019-0590-2⟩. ⟨hal-02268423⟩

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