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Gene augmentation therapy for hereditary retinal degeneration caused by mutations in the PRPF31 gene
Gene augmentation therapy for hereditary retinal degeneration caused by mutations in the PRPF31 gene
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机译:基因扩增治疗PRPF31基因突变引起的遗传性视网膜变性
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摘要
The present invention relates to methods and compositions for gene therapy of retinal pigment degeneration associated with mutations in mRNA precursor processing factor 31 (PRPF31).
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