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Where are the missing gene defects in inherited retinal disorders? : intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders
Journal Contribution - Journal Article
Journal: HUMAN MUTATION
ISSN: 1098-1004
Issue: 6
Volume: 40
Publication year:2019
BOF-keylabel:yes
IOF-keylabel:yes
BOF-publication weight:3
CSS-citation score:1
Authors:International
Authors from:Higher Education
Accessibility:Closed
- Christina Zeitz (Author)
- Christelle Michiels (Author)
- Marion Neuillé (Author)
- Christoph Friedburg (Author)
- Christel Condroyer (Author)
- Fiona Boyard (Author)
- Aline Antonio (Author)
- Nassima Bouzidi (Author)
- Diana Milicevic (Author)
- Robin Veaux (Author)
- Aurore Tourville (Author)
- Axelle Zoumba (Author)
- Imene Seneina (Author)
- Marine Foussard (Author)
- Camille Andrieu (Author)
- Markus N Preising (Author)
- Steven Blanchard (Author)
- Jean-Paul Saraiva (Author)
- Lilia Mesrob (Author)
- Edith Le Floch (Author)
- Claire Jubin (Author)
- Vincent Meyer (Author)
- Helene Blanché (Author)
- Anne Boland (Author)
- Jean-François Deleuze (Author)
- Dror Sharon (Author)
- Isabelle Drumare (Author)
- Sabine Defoort-Dhellemmes (Author)
- Elfride De Baere (Author)
- Bart Leroy (Author)
- Xavier Zanlonghi (Author)
- Ingele Casteels (Author)
- Thorny J de Ravel (Author)
- Irina Balikova (Author)
- Rob K Koenekoop (Author)
- Fanny Laffargue (Author)
- Rebecca McLean (Author)
- Irene Gottlob (Author)
- Dominique Bonneau (Author)
- Daniel F Schordert (Author)
- Francis L Munier (Author)
- Martin McKibbin (Author)
- Katrina Prescott (Author)
- Valerie Pelletier (Author)
- Helene Dollfuss (Author)
- Yaumara Perdomo-Trujillo (Author)
- Celine Faure (Author)
- Charlotte Reiff (Author)
- Bernd Wissinger (Author)
- Isabelle Meunier (Author)
- Susanne Kohl (Author)
- Eyal Banin (Author)
- Eberhart Zrenner (Author)
- Bernhard Jurklies (Author)
- Birgit Lorenz (Author)
- Jose-Alain Sahel (Author)
- Isabelle Audo (Author)
