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Biallelic variants in ADAMTS15 cause a novel form of distal arthrogryposis

  • Felix Boschann
    Affiliations
    Institute of Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany

    RG Development & Disease, Max Planck Institute for Molecular Genetics, Berlin, Germany
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  • Muhsin Ö. Cogulu
    Affiliations
    Department of Pediatric Genetics, Faculty of Medicine, Ege University, Izmir, Turkey
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  • Davut Pehlivan
    Affiliations
    Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX

    Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, TX

    Section of Pediatric Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, TX
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  • Saranya Balachandran
    Affiliations
    Institute of Human Genetics, University of Lübeck, Lübeck, Germany

    Institute of Human Genetics, Kiel University, Kiel, Germany
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  • Pedro Vallecillo-Garcia
    Affiliations
    Institute of Biochemistry, Freie University Berlin, Berlin, Germany
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  • Christopher M. Grochowski
    Affiliations
    Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX
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  • Nils R. Hansmeier
    Affiliations
    Institute of Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany

    RG Development & Disease, Max Planck Institute for Molecular Genetics, Berlin, Germany

    BIH Center for Regenerative Therapies (BCRT), Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany
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  • Zeynep H. Coban Akdemir
    Affiliations
    Department of Epidemiology, Human Genetics and Environmental Science, UTHealth School of Public Health, The University of Texas Houston, TX
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  • Cesar A. Prada-Medina
    Affiliations
    RG Development & Disease, Max Planck Institute for Molecular Genetics, Berlin, Germany
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  • Ayca Aykut
    Affiliations
    Department of Medical Genetics, Faculty of Medicine, Ege University, Izmir, Turkey
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  • Björn Fischer-Zirnsak
    Affiliations
    Institute of Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany

    RG Development & Disease, Max Planck Institute for Molecular Genetics, Berlin, Germany
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  • Simon Badura
    Affiliations
    Interdisciplinary Pediatric Center for Children With Developmental Disabilities and Severe Chronic Disorders, Department of Pediatrics and Adolescent Medicine, University Medical Center Göttingen, Göttingen, Germany
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  • Burak Durmaz
    Affiliations
    Department of Pediatric Genetics, Faculty of Medicine, Ege University, Izmir, Turkey
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  • Ferda Ozkinay
    Affiliations
    Department of Medical Genetics, Faculty of Medicine, Ege University, Izmir, Turkey
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  • René Hägerling
    Affiliations
    Institute of Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany

    RG Development & Disease, Max Planck Institute for Molecular Genetics, Berlin, Germany

    BIH Center for Regenerative Therapies (BCRT), Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany
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  • Jennifer E. Posey
    Affiliations
    Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX
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  • Sigmar Stricker
    Affiliations
    Institute of Biochemistry, Freie University Berlin, Berlin, Germany
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  • Gabriele Gillessen-Kaesbach
    Affiliations
    Institute of Human Genetics, University of Lübeck, Lübeck, Germany
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  • Malte Spielmann
    Affiliations
    Institute of Human Genetics, University of Lübeck, Lübeck, Germany

    Institute of Human Genetics, Kiel University, Kiel, Germany
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  • Denise Horn
    Affiliations
    Institute of Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany
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  • Knut Brockmann
    Affiliations
    Interdisciplinary Pediatric Center for Children With Developmental Disabilities and Severe Chronic Disorders, Department of Pediatrics and Adolescent Medicine, University Medical Center Göttingen, Göttingen, Germany
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  • James R. Lupski
    Affiliations
    Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX

    Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, TX
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  • Uwe Kornak
    Affiliations
    Institute of Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany

    RG Development & Disease, Max Planck Institute for Molecular Genetics, Berlin, Germany

    Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany
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  • Julia Schmidt
    Affiliations
    Institute of Human Genetics, University of Lübeck, Lübeck, Germany

    Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany
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Open AccessPublished:February 28, 2023DOI:https://doi.org/10.1016/j.gim.2023.100799
Biallelic variants in ADAMTS15 cause a novel form of distal arthrogryposis
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      Correction to: Genetics in Medicine 2022; https://doi.org/10.1016/j.gim.2022.07.012, published online 01 October 2022.
      In the article “Biallelic variants in ADAMTS15 cause a novel form of distal arthropryposis” by Boschann F et al (Genet Med 2022;24:2187-2193), the author Ozgur Cogulu’s name was incorrectly listed as “Muhsin Ö. Cogulu” throughout the article. The authors would like to apologize for any inconvenience this may have caused.

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      Published online: February 28, 2023

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      In Press Corrected Proof

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      DOI: https://doi.org/10.1016/j.gim.2023.100799

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