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Autosomal dominant cone–rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D , which encodes retinal guanylate cyclase 1 1The authors have no proprietary interests in the materials mentioned in the study.

Heterozygous MutationOcular DiseaseRetinaPhotoreceptor CellOphthalmologyGeneticsMolecular GeneticsProprietary InterestsGlaucomaRetinal TherapiesMedicine