Publication | Closed Access

Heterozygous missense mutation in the rod cGMP phosphodiesterase β–subunit gene in autosomal dominant stationary night blindness

Ocular DiseaseMolecular NeuroscienceRetinaOphthalmologyPhotoreceptor CellGenetic DisorderGeneticsMolecular GeneticsNeuroscienceRetinal TherapiesMedicineHeterozygous Missense MutationSocial SciencesNeurogenetics