NGS studies were conducted on 24 NDM children from the Oman population, and genetic abnormalities were discovered including KCNJ11 mutations and 6q24 methylation abnormalities using methylation specific PCR and polymorphic loci, as well as mutations in the GCK, LRBA, SLC2A2, and IL2RA genes in 62.5% of the patients (Al Senani et al., 2018). This evidence concerns the gene SLC2A2 and neonatal diabetes mellitus.