Lv1
20 积分 2026-04-13 加入
Antisense oligonucleotide-based treatment of retinitis pigmentosa caused by USH2A exon 13 mutations
4个月前
已完结
Modeling PRPF31 retinitis pigmentosa using retinal pigment epithelium and organoids combined with gene augmentation rescue
4个月前
已完结
Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies
4个月前
已完结
Targeted Next Generation Sequencing Revealed NovelPRPF31Mutations in Autosomal Dominant Retinitis Pigmentosa
4个月前
已完结
Identification of two novel PRPF31 mutations in Chinese families with non‐syndromic autosomal dominant retinitis pigmentosa
4个月前
已完结
Activation of autophagy reverses progressive and deleterious protein aggregation in PRPF31 patient-induced pluripotent stem cell-derived retinal pigment epithelium cells
4个月前
已完结
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