Corrigendum to “Hyperphosphatasia With Seizures, Neurologic Deficit, and Characteristic Facial Features: Five New Patients With Mabry Syndrome” Am J Med Genet 152A: 1661-1669

Authors

  • Miles D. Thompson,

    1. Department of Laboratory Medicine & Pathobiology, University of Toronto, Toronto, ON, Canada
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  • Marjan M. Nezarati,

    1. Division of Clinical and Metabolic Genetics, Hospital for Sick Children, Toronto, ON, Canada
    2. Department of Genetics, North York General Hospital, Toronto, ON, Canada
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  • Gabriele Gillessen-Kaesbach,

    1. Institut für Humangenetik, Universität zu Lübeck, Lübeck, Germany
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  • Peter Meinecke,

    1. Abteilung Medizinische Genetik, Altonaer Kinderkrankenhaus, Hamburg, Germany
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  • Roberto Mendoza-Londono,

    1. Division of Clinical and Metabolic Genetics, Hospital for Sick Children, Toronto, ON, Canada
    2. Department of Pediatrics, University of Toronto, Toronto, ON, Canada
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  • Etienne Mornet,

    1. Laboratoire SESEP, Centre Hospitalier de Versailles, Le Chesnay, France
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  • Isabelle Brun-Heath,

    1. Equipe Structure-Fonction et Génétique, CHU Paris Ile de France Ouest, Université de Versailles-Saint Quentin en Yvelines, Versailles, France
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  • Catherine Prost Squarcioni,

    1. Laboratoire d'Histologie, UFR Léonard de Vinci, Bobigny, France
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  • Laurence Legeai-Mallet,

    1. INSERM U781, Université Paris Descartes, Hôpital Necker-Enfants Malades, Paris, France
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  • Arnold Munnich,

    1. INSERM U781, Université Paris Descartes, Hôpital Necker-Enfants Malades, Paris, France
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  • David E.C. Cole

    Corresponding author
    1. Department of Laboratory Medicine & Pathobiology, University of Toronto, Toronto, ON, Canada
    2. Division of Clinical and Metabolic Genetics, Hospital for Sick Children, Toronto, ON, Canada
    3. Department of Pediatrics, University of Toronto, Toronto, ON, Canada
    4. Department of Clinical Pathology, Sunnybrook & Women's College Health Sciences Centre, Toronto, ON, Canada
    5. Department of Medicine, University of Toronto, Toronto, ON, Canada
    • Rm 415, 100 College St, Toronto, ON, Canada M5G 1L5.
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Errata

This article corrects:

  1. Hyperphosphatasia with seizures, neurologic deficit, and characteristic facial features: Five new patients with Mabry syndrome Volume 152A, Issue 7, 1661–1669, Article first published online: 3 June 2010

  • How to cite this article: Thompson MD, Nezarati MM, Gillessen-Kaesbach G, Meinecke P, Mendoza-Londono R, Mornet E, Brun-Heath I, Squarcioni CP, Legeai-Mallet L, Munnich A, Cole DEC. 2011. Corrigendum to “Hyperphosphatasia with seizures, neurologic deficit, and characteristic facial features: Five new patients with Mabry syndrome” Am J Med Genet 152A: 1661-1669. Am J Med Genet Part A 155:1215.

  • Miles D. Thompson and Marjan M. Nezarati contributed equally to this work.

No abstract is available for this article.

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