065. The Genetic Spectrum and Clinical Features of X-Linked Juvenile Retinoschisis in Central China

yiqi.zhang2023-04-18T17:27:11+08:00

065. The Genetic Spectrum and Clinical Features of X-Linked Juvenile Retinoschisis in Central Chinayiqi.zhang2023-04-18T17:27:11+08:00

058. A Novel Mutation Located in the Intermembrane Space Domain of AFG3L2 Causes Dominant Optic Atrophy Through Decreasing the Stability of the Encoded Protein

yiqi.zhang2023-04-18T17:39:14+08:00

058. A Novel Mutation Located in the Intermembrane Space Domain of AFG3L2 Causes Dominant Optic Atrophy Through Decreasing the Stability of the Encoded Proteinyiqi.zhang2023-04-18T17:39:14+08:00

057. Genotypes and Phenotypes Analysis of a Novel Complex Heterozygous Mutation of CEP290 Related Isolated Cone-Rod Dystrophy

yiqi.zhang2023-04-18T17:42:13+08:00

057. Genotypes and Phenotypes Analysis of a Novel Complex Heterozygous Mutation of CEP290 Related Isolated Cone-Rod Dystrophyyiqi.zhang2023-04-18T17:42:13+08:00

054. Supernormal Rod Response Mediated by a Novel KCNV2 Variant in a Cone Dystrophy Type 3B Patient

yiqi.zhang2023-04-18T17:44:05+08:00

054. Supernormal Rod Response Mediated by a Novel KCNV2 Variant in a Cone Dystrophy Type 3B Patientyiqi.zhang2023-04-18T17:44:05+08:00

053. Retinoblastoma in Adults: Clinical Features, Gene Mutations and Treatment Outcomes: A Study of Six Cases

yiqi.zhang2023-02-13T11:30:32+08:00

053. Retinoblastoma in Adults: Clinical Features, Gene Mutations and Treatment Outcomes: A Study of Six Casesyiqi.zhang2023-02-13T11:30:32+08:00

052. Multi-mtDNA Variants May Be a Factor Contributing to Mitochondrial Function Variety in the Skin-Derived Fibroblasts of Leber’s Hereditary Optic Neuropathy Patients

yiqi.zhang2023-02-13T11:29:44+08:00

052. Multi-mtDNA Variants May Be a Factor Contributing to Mitochondrial Function Variety in the Skin-Derived Fibroblasts of Leber’s Hereditary Optic Neuropathy Patientsyiqi.zhang2023-02-13T11:29:44+08:00

051. Autosomal Dominant Optic Atrophy Caused by Six Novel Pathogenic OPA1 Variants and Genotype-Phenotype Correlation Analysis

yiqi.zhang2023-04-18T17:45:08+08:00

051. Autosomal Dominant Optic Atrophy Caused by Six Novel Pathogenic OPA1 Variants and Genotype-Phenotype Correlation Analysisyiqi.zhang2023-04-18T17:45:08+08:00

049. Vitreoretinal Amyloidosis: Clinical Features, OCTA Appearances, Gene Mutations, and Treatment Outcomes of Vitrectomy Surgery

yiqi.zhang2023-02-13T11:25:28+08:00

049. Vitreoretinal Amyloidosis: Clinical Features, OCTA Appearances, Gene Mutations, and Treatment Outcomes of Vitrectomy Surgeryyiqi.zhang2023-02-13T11:25:28+08:00

029. Phenotype Heterogeneity and the Association Between Visual Acuity and Outer Retinal Structure in a Cohort of Chinese X-Linked Juvenile Retinoschisis Patients

yiqi.zhang2023-02-13T10:51:31+08:00

029. Phenotype Heterogeneity and the Association Between Visual Acuity and Outer Retinal Structure in a Cohort of Chinese X-Linked Juvenile Retinoschisis Patientsyiqi.zhang2023-02-13T10:51:31+08:00

012. Autosomal Recessive Retinitis Pigmentosa Associated with Three Novel REEP6 Variants in Chinese Population

yiqi.zhang2023-02-10T15:55:59+08:00

012. Autosomal Recessive Retinitis Pigmentosa Associated with Three Novel REEP6 Variants in Chinese Populationyiqi.zhang2023-02-10T15:55:59+08:00