PublisherDOIYearVolumeIssuePageTitleAuthor(s)Link
Endocrinology and Metabolism10.3803/enm.2021.2022021362468Identification of Maturity-Onset Diabetes of the Young Caused by Glucokinase Mutations Detected Using Whole-Exome SequencingEun-Hee Cho, Jae Woong Min, Sun Shim Choi, Hoon Sung Choi, Sang-Wook Kimhttp://e-enm.org/upload/pdf/enm-2021-202.pdf, http://e-enm.org/journal/view.php?doi=10.3803/EnM.2021.202, http://e-enm.org/upload/pdf/enm-2021-202.pdf
Endocrinology and Metabolism10.3803/enm.2017.32.2.2962017322296Identification of Maturity-Onset Diabetes of the Young Caused by Glucokinase Mutations Detected Using Whole-Exome SequencingEun-Hee Cho, Jae Woong Min, Sun Shim Choi, Hoon Sung Choi, Sang-Wook Kimhttps://synapse.koreamed.org/pdf/10.3803/EnM.2017.32.2.296, https://synapse.koreamed.org/DOIx.php?id=10.3803/EnM.2017.32.2.296, https://synapse.koreamed.org/DOIx.php?id=10.3803/EnM.2017.32.2.296
Frontiers in Endocrinology10.3389/fendo.2020.534362202111Identification of Maturity-Onset Diabetes of the Young Caused by Mutation in FOXM1 via Whole-Exome Sequencing in Northern ChinaLiang Zhong, Zengyi Zhao, Qingshan Hu, Yang Li, Weili Zhao, Chuang Li, Yunqiang Xu, Ruijuan Rong, Jing Zhang, Zifeng Zhang, Nan Li, Zanchao Liuhttps://www.frontiersin.org/articles/10.3389/fendo.2020.534362/full
The Lancet10.1016/0140-6736(92)91768-419923408817444-448Primary pancreatic beta-cell secretory defect caused by mutations in glucokinase gene in kindreds of maturity onset diabetes of the youngG VELHOhttps://api.elsevier.com/content/article/PII:0140-6736(92)91768-4?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:0140-6736(92)91768-4?httpAccept=text/plain
10.21203/rs.3.rs-41775/v22020Identification of Novel Gene Mutations in Degenerative Lumbar Spinal Stenosis Using Whole Exome Sequencing in Chinese PopulationXin Jiang, Dong Chenhttps://www.researchsquare.com/article/rs-41775/v2, https://www.researchsquare.com/article/rs-41775/v2.html
10.21203/rs.3.rs-41775/v12020Identification of Novel Gene Mutations in Degenerative Lumbar Spinal Stenosis Using Whole Exome Sequencing in Chinese PopulationXin Jiang, Dong Chenhttps://www.researchsquare.com/article/rs-41775/v1, https://www.researchsquare.com/article/rs-41775/v1.html
Human Mutation10.1002/humu.102772003225353-362Glucokinase (GCK) mutations in hyper- and hypoglycemia: Maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancyAnna L. Gloynhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fhumu.10277, https://onlinelibrary.wiley.com/doi/full/10.1002/humu.10277
Diabetes10.2337/db20-1550-p202069Supplement 11550-P1550-P: Whole-Exome Sequencing in Children with Suspected Maturity-Onset Diabetes of the Young (MODY)MUSTAFA TOSUR, ANIKO SABO, MICHAEL M. KHAYAT, SHALINI N. JHANGIANI, AHMAD K. REFAEY, DONNA MUZNY, RICHARD A. GIBBS, ASHOK BALASUBRAMANYAM, MARIA J. REDONDOhttps://syndication.highwire.org/content/doi/10.2337/db20-1550-P
Human Mutation10.1002/humu.91792003224338-338Identification of eight novel glucokinase mutations in Italian children with maturity-onset diabetes of the youngVilma Mantovani, Silvana Salardi, Vincenzo Cerreta, Daniela Bastia, Marinella Cenci, Luca Ragni, Stefano Zucchini, Raffaele Parente, Alessandro Cicognanihttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fhumu.9179, https://onlinelibrary.wiley.com/doi/full/10.1002/humu.9179
Human Mutation10.1002/humu.91862003225417-417Identification of 21 novel glucokinase (GCK) mutations in UK and European Caucasians with maturity-onset diabetes of the young (MODY)K.L. Thomson, A.L. Gloyn, K. Colclough, M. Batten, L.I.S. Allen, F. Beards, A.T. Hattersley, S. Ellardhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fhumu.9186, https://onlinelibrary.wiley.com/doi/full/10.1002/humu.9186