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American Diabetes Association            Professional Practice Committee. 2. Classification and            diagnosis of diabetes: standards of medical care in diabetes-2022.            Diabetes Care          2022;45(Suppl 1):            S17\u201338.","DOI":"10.2337\/dc22-S002"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Bonnefond,                A,              Philippe, J,                Durand, E,                Dechaume,            A, Huyvaert,                M,              Montagne, L,              et al. Whole-exome sequencing and high            throughput genotyping identified <i>KCNJ11<\/i> as the thirteenth MODY            gene. PLoS One          2012;7: e37423.","DOI":"10.1371\/journal.pone.0037423"},{"key":"3","unstructured":"3. Kitamyama,                K,              Watanabe, Y,                Yamada, Y,                Higuchi, S,                Isaka, Y,                Motoyama,            K, et al.            Effective management of hyperglycemia with relatively high-dose            glibenclamide in a case of young-onset KATP-channel diabetes mellitus.            J Japan Diab Soc          2022;65: 658\u201364(in            Japanese)."},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Yorifuji,                T,                Nagashima,              K, Kurokawa,                K, Kawai,                M, Oishi,                M, Akazawa,                Y, et al.            The C42R mutation in the Kir6.2 (<i>KCNJ11<\/i>) gene as a cause            of transient neonatal diabetes, childhood diabetes, or later-onset, apparently type 2            diabetes mellitus. J Clin Endocrinol Metab          2005;90: 3174\u20138.","DOI":"10.1210\/jc.2005-0096"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Gloyn,              AL, Pearson,                ER,                Antcliff,              JF, Proks,                P,              Bruining, GJ,                Slingerland,              AS, et al.            Activating mutations in the gene encoding the ATP-sensitive            potassium-channel subunit Kir6.2 and permanent neonatal diabetes.            N Engl J Med          2004;350: 1838\u201349.","DOI":"10.1056\/NEJMoa032922"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Chen,              Y, Hu,                X, Cui,                J, Zhao,                M, Yao,                H. A novel            mutation <i>KCNJ11<\/i> R136C caused            <i>KCNJ11<\/i>-MODY. Diabetol Metab Syndr          2021;13: 91.","DOI":"10.1186\/s13098-021-00708-6"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. De                Franco, E,                Saint-Martin,              C, Brusgaard,                K, Knight                Johnson, AE,                Aguilar-Bryan,              L, Bowman,                P, et al.            Update of variants identified in the pancreatic \u03b2-cell K<sub>ATP<\/sub>            channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and            diabetes. Hum Mutat          2020;41: 884\u2013905.","DOI":"10.1002\/humu.23995"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Richards,                S, Aziz,                N, Bale,                S, Bick,                D, Das,                S,                Gastier-Foster,              J, et al.            ACMG Laboratory Quality Assurance Committee.            Standards and guidelines for the interpretation of sequence variants: a            joint consensus recommendation of the American College of Medical Genetics and Genomics            and the Association for Molecular Pathology. Genet Med          2015;17: 405\u201324.","DOI":"10.1038\/gim.2015.30"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Adzhubei,                IA,              Schmidt, S,                Peshkin, L,                Ramensky,              VE,                Gerasimova,              A, Bork,                P, et al.            A method and server for predicting damaging missense            mutations. Nat Methods          2010;7: 248\u20139.","DOI":"10.1038\/nmeth0410-248"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Antcliff,                JF, Haider,                S, Proks,                P, Sansom,                MS,                Ashcroft,              FM. Functional            analysis of a structural model of the ATP-binding site of the KATP channel Kir6.2            subunit. EMBO J          2005;24: 229\u201339.","DOI":"10.1038\/sj.emboj.7600487"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Bowman,              P, Sulen,                \u00c5,              Barbetti, F,                Beltrand,            J, Svalastoga,                P, Codner,                E, et al.            Neonatal Diabetes International Collaborative Group.            Effectiveness and safety of long-term treatment with sulfonylureas in            patients with neonatal diabetes due to <i>KCNJ11<\/i> mutations: an            international cohort study. Lancet Diabetes Endocrinol          2018;6: 637\u201346.","DOI":"10.1016\/S2213-8587(18)30106-2"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Warncke,              K, Eckert,                A,              Kapellen, T,                Kummer, S,                Raile, K,                Dunstheimer,              D, et al.            Clinical presentation and long-term outcome of patients with              <i>KCNJ11<\/i>\/ABCC8 variants: Neonatal diabetes or MODY in the DPV registry            from Germany and Austria. Pediatr Diabetes          2022;23: 999\u20131008.","DOI":"10.1111\/pedi.13390"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Pearson,                ER,                Flechtner,              I, Nj\u00f8lstad,                PR,              Malecki, MT,                Flanagan,              SE, Larkin,                B, et al.            Neonatal Diabetes International Collaborative Group.            Switching from insulin to oral sulfonylureas in patients with diabetes            due to Kir6.2 mutations. N Engl J Med          2006;355: 467\u201377.","DOI":"10.1056\/NEJMoa061759"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Garcin,              L, Mericq,                V,                Fauret-Amsellem,              AL, Cave,                H, Polak,                M,              Beltrand,            J. Neonatal            diabetes due to potassium channel mutation: Response to sulfonylurea according to the            genotype. Pediatr Diabetes          2020;21: 932\u201341.","DOI":"10.1111\/pedi.13041"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Babiker,              T, Vedovato,                N, Patel,                K, Thomas,                N, Finn,                R,              M\u00e4nnikk\u00f6, R,              et al. Successful transfer to sulfonylureas            in <i>KCNJ11<\/i> neonatal diabetes is determined by the mutation and duration            of diabetes. Diabetologia          2016;59: 1162\u20136.","DOI":"10.1007\/s00125-016-3921-8"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Thurber,                BW,              Carmody, D,                Tadie, EC,                Pastore,            AN, Dickens,                JT,                Wroblewski,              KE, et al.            United States Neonatal Diabetes Working Group.            Age at the time of sulfonylurea initiation influences treatment outcomes            in <i>KCNJ11<\/i>-related neonatal diabetes.            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