103.Pathogenicity and Function Analysis of Two Novel SLC4A11 Variants in Patients With Congenital Hereditary Endothelial Dystrophy yuping.zhou2024-11-05T17:21:38+08:00 103.Pathogenicity and Function Analysis of Two Novel SLC4A11 Variants in Patients With Congenital Hereditary Endothelial Dystrophyyuping.zhou2024-11-05T17:21:38+08:00
