Cite

    Tourville, A., Michiels, C., Condroyer, C., Meunier, A., Cordonnier, M., Sahel, J., Audo, I., Abramowicz, M., & Zeitz, C. (2019). identification of a novel GRM6 mutation in a previously described consanguineous family with complete congenital stationary night blindness. Ophthalmic genetics, 40, 182–184. http://access.bl.uk/ark:/81055/vdc_100081481880.0x000036