Publication | Open Access
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness
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Citations
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References
2012
Year
Ocular DiseaseDevelopmental BiologyMendelian DisorderOphthalmologyGenetic DisorderGeneticsClinical GeneticsMedicineNeurogenetics
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