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Research Article

The R403Q Myosin Mutation Implicated in Familial Hypertrophic Cardiomyopathy Causes Disorder at the Actomyosin Interface

  • Niels Volkmann,

    Affiliation: Burnham Institute for Medical Research, La Jolla, California, United States of America

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  • HongJun Lui,

    Affiliation: Burnham Institute for Medical Research, La Jolla, California, United States of America

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  • Larnele Hazelwood,

    Affiliation: Burnham Institute for Medical Research, La Jolla, California, United States of America

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  • Kathleen M. Trybus,

    Affiliation: Department of Molecular Physiology and Biophysics, University of Vermont, Burlington, Vermont, United States of America

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  • Susan Lowey mail,

    To whom correspondence should be addressed. E-mail: Susan.Lowey@uvm.edu (SL); dorit@burnham.org (DH)

    Affiliation: Department of Molecular Physiology and Biophysics, University of Vermont, Burlington, Vermont, United States of America

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  • Dorit Hanein mail

    To whom correspondence should be addressed. E-mail: Susan.Lowey@uvm.edu (SL); dorit@burnham.org (DH)

    Affiliation: Burnham Institute for Medical Research, La Jolla, California, United States of America

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  • Published: November 07, 2007
  • DOI: 10.1371/journal.pone.0001123

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