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Publisher Correction: Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis

Author

Listed:
  • Nina K. Serwas

    (Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases
    CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
    University of California San Francisco)

  • Birgit Hoeger

    (Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases
    CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
    St. Anna Children’s Cancer Research Institute (CCRI))

  • Rico C. Ardy

    (Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases
    CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences)

  • Sigrun V. Stulz

    (Karolinska University Hospital Huddinge)

  • Zhenhua Sui

    (La Jolla Institute for Allergy & Immunology)

  • Nima Memaran

    (Medical University of Vienna
    Hannover Medical School)

  • Marie Meeths

    (Karolinska University Hospital Solna
    Karolinska University Hospital Solna)

  • Ana Krolo

    (Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases
    CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences)

  • Özlem Yüce Petronczki

    (Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases
    CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences)

  • Laurène Pfajfer

    (Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases
    CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
    Paul Sabatier University)

  • Tie Z. Hou

    (Royal Free Hospital)

  • Neil Halliday

    (Royal Free Hospital)

  • Elisangela Santos-Valente

    (CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences)

  • Artem Kalinichenko

    (Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases
    CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences)

  • Alan Kennedy

    (Royal Free Hospital)

  • Emily M. Mace

    (Texas Children’s Hospital
    Columbia University Medical Center)

  • Malini Mukherjee

    (Texas Children’s Hospital)

  • Bianca Tesi

    (Karolinska University Hospital Solna)

  • Anna Schrempf

    (CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences)

  • Winfried F. Pickl

    (Medical University of Vienna)

  • Joanna I. Loizou

    (CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences)

  • Renate Kain

    (Medical University of Vienna)

  • Bettina Bidmon-Fliegenschnee

    (Medical University of Vienna)

  • Jean-Nicolas Schickel

    (Yale University School of Medicine)

  • Salomé Glauzy

    (Yale University School of Medicine)

  • Jakob Huemer

    (Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases
    CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences)

  • Wojciech Garncarz

    (Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases
    CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences)

  • Elisabeth Salzer

    (Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases
    CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences)

  • Iro Pierides

    (Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases
    CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences)

  • Ivan Bilic

    (CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
    Takeda (Shire))

  • Jens Thiel

    (University Medical Center Freiburg)

  • Peter Priftakis

    (Karolinska University Hospital Huddinge)

  • Pinaki P. Banerjee

    (Texas Children’s Hospital
    MD Anderson Cancer Center)

  • Elisabeth Förster-Waldl

    (Medical University of Vienna)

  • David Medgyesi

    (Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases
    CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences)

  • Wolf-Dietrich Huber

    (Medical University of Vienna)

  • Jordan S. Orange

    (Texas Children’s Hospital
    Columbia University Medical Center)

  • Eric Meffre

    (Yale University School of Medicine)

  • David M. Sansom

    (Royal Free Hospital)

  • Yenan T. Bryceson

    (Karolinska University Hospital Huddinge)

  • Amnon Altman

    (La Jolla Institute for Allergy & Immunology)

  • Kaan Boztug

    (Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases
    CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
    St. Anna Children’s Cancer Research Institute (CCRI)
    Medical University of Vienna)

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Suggested Citation

  • Nina K. Serwas & Birgit Hoeger & Rico C. Ardy & Sigrun V. Stulz & Zhenhua Sui & Nima Memaran & Marie Meeths & Ana Krolo & Özlem Yüce Petronczki & Laurène Pfajfer & Tie Z. Hou & Neil Halliday & Elisang, 2019. "Publisher Correction: Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis," Nature Communications, Nature, vol. 10(1), pages 1-2, December.
    • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-12454-5
    DOI: 10.1038/s41467-019-12454-5
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