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
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
