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Newly Identified Genetic Variants Associated with Specific Phenotypes of Diabetic Retinopathy. (A) Enrichment of the ‘risk’ allele in five candidate genes in cases of advanced PDR patients revealed a disruptive in-frame deletion and four heterozygous missense variants. (B) A variant in the NKX2.3 gene was shared in the “extreme” DR phenotype (No DR) group.
