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De                Franco, E,                Flanagan,              SE, Houghton,                JA, Lango                Allen, H,                Mackay, DJ,                Temple, IK,              et al. The effect of early, comprehensive            genomic testing on clinical care in neonatal diabetes: an international cohort            study. Lancet          2015;386: 957\u201363.","DOI":"10.1016\/S0140-6736(15)60098-8"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Ellard,              S, Lango                Allen, H,                De Franco,              E, Flanagan,                SE,              Hysenaj, G,                Colclough,              K, et al.            Improved genetic testing for monogenic diabetes using targeted            next-generation sequencing. Diabetologia          2013;56: 1958\u201363.","DOI":"10.1007\/s00125-013-2962-5"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. 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":"4","doi-asserted-by":"crossref","unstructured":"4. Letourneau,                LR,              Carmody, D,                Wroblewski,              K, Denson,                AM,                Sanyoura,            M, Naylor,                RN, et al.            Diabetes presentation in infancy: high risk of diabetic            ketoacidosis. Diabetes Care          2017;40: e147\u20138.","DOI":"10.2337\/dc17-1145"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Edghill,                EL,                Flanagan,              SE, Ellard,                S. Permanent            neonatal diabetes due to activating mutations in ABCC8 and KCNJ11.            Rev Endocr Metab Disord          2010;11: 193\u20138.","DOI":"10.1007\/s11154-010-9149-x"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Rubio-Cabezas,                O,              Flanagan, SE,                Damhuis, A,                Hattersley,              AT, Ellard,                S. KATP            channel mutations in infants with permanent diabetes diagnosed after 6 months of            life. Pediatr Diabetes          2012;13: 322\u20135.","DOI":"10.1111\/j.1399-5448.2011.00824.x"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Mohamadi,                A, Clark,                LM, Lipkin,                PH, Mahone,                EM, Wodka,                EL,                Plotnick,              LP. Medical and            developmental impact of transition from subcutaneous insulin to oral glyburide in a            15-yr-old boy with neonatal diabetes mellitus and intermediate DEND syndrome: extending            the age of KCNJ11 mutation testing in neonatal DM. Pediatr            Diabetes          2010;11: 203\u20137.","DOI":"10.1111\/j.1399-5448.2009.00548.x"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Yorifuji,                T,                Nagashima,              K, Kurokawa,                K, Kawai,                M, Oishi,                M, Akazawa,                Y, et al.            The C42R mutation in the Kir6.2 (KCNJ11) 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":"9","doi-asserted-by":"crossref","unstructured":"9. Lin,              Y, Sheng,                H, Ting,                TH, Xu,                A, Yin,                X, Cheng,                J, et al.            Molecular and clinical characteristics of monogenic diabetes mellitus in            southern Chinese children with onset before 3 years of age. BMJ            Open Diabetes Res Care          2020;8: e001345.","DOI":"10.1136\/bmjdrc-2020-001345"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Gloyn,              AL,                Diatloff-Zito,              C, Edghill,                EL,                Bellann\u00e9-Chantelot,              C, Nivot,                S, Coutant,                R, et al.            KCNJ11 activating mutations are associated with developmental delay,            epilepsy and neonatal diabetes syndrome and other neurological features.            Eur J Hum Genet          2006;14: 824\u201330.","DOI":"10.1038\/sj.ejhg.5201629"},{"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 KCNJ11 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. Hattersley,                AT,              Greeley, SAW,                Polak, M,                Rubio-Cabezas,              O, Nj\u00f8lstad,                PR,                Mlynarski,              W, et al.            ISPAD Clinical Practice Consensus Guidelines 2018: The diagnosis and            management of monogenic diabetes in children and adolescents.            Pediatr Diabetes          2018;19(Suppl 27):            47\u201363.","DOI":"10.1111\/pedi.12772"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. St\u00f8y,              J, Greeley,                SAW, Paz,                VP, Ye,                H, Pastore,                AN,              Skowron, KB,              et al. United States Neonatal Diabetes            Working Group. Diagnosis and treatment of neonatal            diabetes: a United States experience. 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