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Null mutation in the human 11-cis retinol dehydrogenase gene associated with fundus albipunctatus11The authors have no proprietary interest in any of the materials used in this study.

Fundus Albipunctatus11the AuthorsOcular DiseaseOphthalmologyGenetic DisorderGeneticsBiochemical GeneticsMolecular GeneticsNull MutationProprietary InterestMedicine