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Matsutani,                N, Furuta,                H, Matsuno,                S, Oku,                Y, Morita,                S, Uraki,                S, et al.            Identification of a compound heterozygous inactivating ABCC8 gene            mutation responsible for young-onset diabetes with exome sequencing.            J Diabetes Investig          2020;11: 333\u20136.","DOI":"10.1111\/jdi.13138"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Perge,              K, Nicolino,                M. Variable            phenotypes of individual and family monogenic cases with hyperinsulinism and diabetes: a            systematic review. Rev Endocr Metab Disord          2022;23: 1063\u201378.","DOI":"10.1007\/s11154-022-09749-2"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Karatojima,                M, Furuta,                H,                Matsutani,              N, Matsuno,                S, Tamai,                M, Komiya,                K, et al.            A family in which people with a heterozygous ABCC8 gene mutation            (p.Lys1385Gln) have progressed from hyperinsulinemic hypoglycemia to            hyperglycemia. J Diabetes          2020;12: 21\u20134.","DOI":"10.1111\/1753-0407.12990"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Nestorowicz,                A, Glaser,                B, Wilson,                BA, Shyng,                SL,              Nichols, CG,                Stanley,            CA, et al.            Genetic heterogeneity in familial hyperinsulinism.            Hum Mol Genet          1998;7: 1119\u201328.","DOI":"10.1093\/hmg\/7.7.1119"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Suchi,              M, MacMullen,                CM,                Thornton,              PS, Adzick,                NS,              Ganguly, A,                Ruchelli,              ED, et al.            Molecular and immunohistochemical analyses of the focal form of            congenital hyperinsulinism. Mod Pathol          2006;19: 122\u20139.","DOI":"10.1038\/modpathol.3800497"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Sogno                Valin, P,                Proverbio,              MC, Diceglie,                C, Gessi,                A, di                Candia, S,                Mariani, B,              et al. Genetic analysis of Italian patients            with congenital hyperinsulinism of infancy. Horm Res            Paediatr          2013;79: 236\u201342.","DOI":"10.1159\/000350827"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Faletra,              F,                Athanasakis,              E, Morgan,                A, Biarn\u00e9s,                X,                Fornasier,              F, Parini,                R, et al.            Congenital hyperinsulinism: clinical and molecular analysis of a large            Italian cohort. Gene          2013;521: 160\u20135.","DOI":"10.1016\/j.gene.2013.03.021"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Popp,              MW, Maquat,                LE.            Organizing principles of mammalian nonsense-mediated mRNA            decay. Annu Rev Genet          2013;47: 139\u201365.","DOI":"10.1146\/annurev-genet-111212-133424"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Billings,                LK, Shi,                Z,                Resurreccion,              WK, Wang,                CH, Wei,                J, Pollin,                TI, et al.            Statistical evidence for high-penetrance MODY-causing genes in a large            population-based cohort. Endocrinol Diabetes Metab          2022;5: e372.","DOI":"10.1002\/edm2.372"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Pinney,              SE,              MacMullen, C,                Becker, S,                Lin, YW,                Hanna, C,                Thornton,            P, et al.            Clinical characteristics and biochemical mechanisms of congenital            hyperinsulinism associated with dominant KATP channel mutations.            J Clin Invest          2008;118: 2877\u201386.","DOI":"10.1172\/JCI35414"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Yorifuji,                T,              Watanabe, Y,                Kitayama,            K, Yamada,                Y, Higuchi,                S, Mori,                J, et al.            Targeted gene panel analysis of Japanese patients with maturity-onset            diabetes of the young-like diabetes mellitus: Roles of inactivating variants in the            ABCC8 and insulin resistance genes. J Diabetes Investig          2023;14: 387\u2013403.","DOI":"10.1111\/jdi.13957"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Li,                M, Gong,                S, Han,                X, Zhang,                S, Ren,                Q, Cai,                X, et al.            Genetic variants of ABCC8 and phenotypic features in Chinese early onset            diabetes. 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