Publication | Open Access
Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness
60
Citations
69
References
2016
Year
Biallelic MutationsGnb3 CauseMendelian DisorderOphthalmologyGenetic DisorderGeneticsGlaucomaUnique FormMedicineNeurogenetics
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