Figure 1From: Genetic diagnosis of X-linked dominant hypophosphatemic rickets in a cohort study: Tubular reabsorption of phosphate and 1,25(OH)2D serum levels are associated with PHEX mutation type Schematic representation of the PHEX gene with the localization of the mutations found in this study. Horizontal lines represent the extention of gross deletions. GenBank ID: NM_000444.4Back to article page