Skip to main content
. 2024 Sep 27;2024(3):24-0065. doi: 10.1530/EDM-24-0065

Figure 1.

Figure 1

Mutation analysis of the solute carrier family 5 member 2 (SLC5A2) gene in the patient. Screenshot from ‘Alamut Visual Plus’. The position of the heterozygous c.469-1G>A likely pathogenic variant is indicated in red.