Lv1
79 积分 2025-07-21 加入
Frequency and clinical pattern of vitelliform macular dystrophy caused by mutations of interphotoreceptor matrix IMPG1 and IMPG2 genes
2个月前
已完结
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes
3个月前
已完结
Hyperactive microtubule binding of RP1L1 (R45W) underlies retinal degeneration and is suppressed by glycerol
3个月前
已关闭
AAVLINK: A potent DNA-recombination method for large cargo delivery in gene therapy
3个月前
已完结
Genetic landscape of hereditary cardiomyopathies and arrhythmias in China
4个月前
已完结
Clinical and Molecular Characterization ofPROM1-Related Retinal Degeneration
9个月前
已完结
Deep phenotyping of PROM1-associated retinal degeneration
9个月前
已完结
Stem cell-based therapies for retinal diseases: focus on clinical trials and future prospects
9个月前
已完结
Post-transplant cyclophosphamide, abatacept, and vedolizumab to prevent GVHD after hematopoietic stem cells transplantation in children with acute leukemia: results of a prospective trial
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