Phenotype-genotype correlation with Sanger sequencing identified retinol dehydrogenase 12 (RDH12) compound heterozygous variants in a Chinese family with Leber congenital amaurosis
Yun Li(Nanjing University of Chinese Medicine), Yangshun Gu(First Affiliated Hospital Zhejiang University), Qing Pan(Zhejiang University of Technology)
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