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Research Article

Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes

  • Dawn E. Watkins-Chow,

    Affiliation: National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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  • Joanna Cooke,

    Affiliation: Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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  • Ruth Pidsley,

    Affiliation: Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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  • Andrew Edwards,

    Affiliation: Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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  • Rebecca Slotkin,

    Affiliation: National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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  • Karen E. Leeds,

    Affiliation: National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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  • Raymond Mullen,

    Affiliation: National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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  • Laura L. Baxter,

    Affiliation: National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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  • Thomas G. Campbell,

    Affiliation: Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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  • Marion C. Salzer,

    Affiliation: Institute of Molecular Pathology, Vienna, Austria

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  • Laura Biondini,

    Affiliation: Department of Biology, University of Rome Tor Vergata, Roma, Italy

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  • Gretchen Gibney,

    Affiliation: National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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  • Françoise Phan Dinh Tuy,

    Affiliation: Institut Cochin, Université Paris Descartes, CNRS (UMR 8104), Paris, France

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  • Jamel Chelly,

    Affiliation: Institut Cochin, Université Paris Descartes, CNRS (UMR 8104), Paris, France

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  • H. Douglas Morris,

    Affiliation: National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, United States of America

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  • Johannes Riegler,

    Affiliation: Centre for Advanced Biomedical Imaging, Department of Medicine and Institute of Child Health, University College London, London, United Kingdom

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  • Mark F. Lythgoe,

    Affiliation: Centre for Advanced Biomedical Imaging, Department of Medicine and Institute of Child Health, University College London, London, United Kingdom

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  • Ruth M. Arkell,

    Affiliation: Early Mammalian Development Laboratory, Research School of Biology, College of Medicine, Biology, and Environment, Australian National University, Canberra, Australia

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  • Fabrizio Loreni,

    Affiliation: Department of Biology, University of Rome Tor Vergata, Roma, Italy

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  • Jonathan Flint,

    Affiliation: Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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  • William J. Pavan equal contributor mail,

    equal contributor Contributed equally to this work with: William J. Pavan, David A. Keays

    bpavan@nhgri.nih.gov

    Affiliation: National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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  • David A. Keays equal contributor

    equal contributor Contributed equally to this work with: William J. Pavan, David A. Keays

    Affiliation: Institute of Molecular Pathology, Vienna, Austria

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  • Published: January 31, 2013
  • DOI: 10.1371/journal.pgen.1003094

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