Skip to Main Content

Paper Details

Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degeneration.
Sci Rep
23
2017
Author NameAffiliation
Shyamanga BorooahMedical Research Council Centre for Regenerative Medicine, University of Edinburgh
Shyamanga Borooah
Camilla DrakeMedical Research Council Human Genetics Unit, Medical Research Council Institute of Genetics and Molecular Medicine, University of Edinburgh
Jayashree SahniUniversity of Liverpool
Jayashree SahniRoche Pharma Research and Early Development, F. Hoffmann-La Roche Ltd
Artur V CideciyanScheie Eye Institute, University of Pennsylvania
Veronique VitartMedical Research Council Human Genetics Unit, Medical Research Council Institute of Genetics and Molecular Medicine, University of Edinburgh
Samuel G JacobsonScheie Eye Institute, University of Pennsylvania
Alan F WrightMedical Research Council Human Genetics Unit, Medical Research Council Institute of Genetics and Molecular Medicine, University of Edinburgh
Caroline HaywardMedical Research Council Human Genetics Unit, Medical Research Council Institute of Genetics and Molecular Medicine, University of Edinburgh
  • 1 - 10

Datasets