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  • ARVO Annual Meeting Abstract June 2017

    CC2D2A mutations lead to variable phenotypes in a family with retinal dystrophy

    Cécile Méjécase; Saddek Mohand-Said; Camille Andrieux; Aurélie Hummel; Saïd El Shamieh; Aline Antonio; Fiona Boyard; Christel Condroyer; Christelle Michiels; Steven Blanchard; Mélanie Letexier; Jean-Paul Saraiva; Jose Alain Sahel; Christina Zeitz; Isabelle S Audo

    Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):573.