Figure 4From: A novel MIPgene mutation associated with autosomal dominant congenital cataracts in a Chinese family The structural model of the MIP protein. A: A structural homology model of the wild-type human MIP protein is displayed. B: A structural alteration of the mutant MIP is displayed. 151 amino acids are truncated from the COOH-terminus of MIP as a result of c.337C > T mutation.Back to article page