Cone Dystrophy with Supernormal Rod Response Is Strictly Associated with Mutations in<i>KCNV2</i>

DOI Web Site 被引用文献5件
  • Bernd Wissinger
    From the Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University Clinics Tu¨bingen, Germany; the
  • Susann Dangel
    From the Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University Clinics Tu¨bingen, Germany; the
  • Herbert Ja¨gle
    University Eye Hospital, Centre for Ophthalmology, University Clinics Tu¨bingen, Germany;
  • Lars Hansen
    The Wilhelm Johannsen Centre for Functional Genome Research, Department of Cellular and Molecular Medicine, University of Copenhagen, Denmark; the
  • Britta Baumann
    From the Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University Clinics Tu¨bingen, Germany; the
  • Gu¨nther Rudolph
    University Eye Hospital, Munich, Germany; the
  • Christiane Wolf
    From the Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University Clinics Tu¨bingen, Germany; the
  • Michael Bonin
    Department of Medical Genetics, Institute for Human Genetics, University Tu¨bingen, Germany; and the
  • Katja Koeppen
    From the Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University Clinics Tu¨bingen, Germany; the
  • Thomas Ladewig
    From the Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University Clinics Tu¨bingen, Germany; the
  • Susanne Kohl
    From the Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University Clinics Tu¨bingen, Germany; the
  • Eberhart Zrenner
    University Eye Hospital, Centre for Ophthalmology, University Clinics Tu¨bingen, Germany;
  • Thomas Rosenberg
    Gordon Norrie Centre for Genetic Eye Diseases, Kennedy Institute–National Eye Clinic, Hellerup, Denmark.

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