Identification of a novel GRM6 mutation in a previously described consanguineous family with complete congenital stationary night blindness.

Identification of a novel GRM6 mutation in a previously described consanguineous family with complete congenital stationary night blindness. Ophthalmic Genet. 2019 Apr;40(2):182-184 Authors: Tourville A, Michiels C, Condroyer C, Meunier A, Cordonnier M, Sahel JA, Audo I, Abramowicz M, Zeitz C PMID: 31063016 [PubMed - in process]
Source: Ophthalmic Genetics - Category: Opthalmology Tags: Ophthalmic Genet Source Type: research