Genotyping Microarray (Disease Chip) for Leber Congenital Amaurosis: Detection of Modifier Alleles

  • Jana Zernant
    From the Departments of Ophthalmology and
  • Maigi Ku¨lm
    Asper Biotech, Ltd., Tartu, Estonia;
  • Sharola Dharmaraj
    Department of Pediatric Ophthalmology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, Massachusetts; the
  • Anneke I. den Hollander
    Department of Human Genetics, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands;
  • Isabelle Perrault
    Ho^pital Des Enfants Malades, Paris, France; the
  • Markus N. Preising
    Department of Pediatric Ophthalmology, Strabismology and Ophthalmogenetics, Klinikum, University of Regensburg, Regensburg, Germany; the
  • Birgit Lorenz
    Department of Pediatric Ophthalmology, Strabismology and Ophthalmogenetics, Klinikum, University of Regensburg, Regensburg, Germany; the
  • Josseline Kaplan
    Ho^pital Des Enfants Malades, Paris, France; the
  • Frans P. M. Cremers
    Department of Human Genetics, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands;
  • Irene Maumenee
    Johns Hopkins University, Baltimore, Maryland; and the
  • Robert K. Koenekoop
    Montreal Children’s Hospital, McGill University Health Center, Montreal, Quebec, Canada.
  • Rando Allikmets
    From the Departments of Ophthalmology and10Pathology, Columbia University, New York, New York;

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