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. 2021 Jul 29;12:684018. doi: 10.3389/fendo.2021.684018

Figure 1.

Figure 1

Clinical and genetic characterization of Tunisian MODY patients reported in previous studies. The clinical and familial inclusion criteria were specific for each study. Pathogenic variants and polymorphisms found in Tunisian patients were mainly reported in the most prevalent MODY genes. Functional studies have not been performed. OHA, oral hypoglycemic agents.