Fig. 2From: Clinical, genetic profile and therapy evaluation of 11 Chinese pediatric patients with Fanconi-Bickel syndromeVariants of SLC2A2 gene identified in 11 patients with FBS. The SLC2A2 variants were depicted as nucleotide alterations and amino acid alterations per exon/intron. The white boxes indicated exons. Novel variants were marked with an asterisk. The suffixes indicated the number of mutant allelesBack to article page