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Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.
Edghill EL, Flanagan SE, Patch AM, Boustred C, Parrish A, Shields B, Shepherd MH, Hussain K, Kapoor RR, Malecki M, MacDonald MJ, Støy J, Steiner DF, Philipson LH, Bell GI; Neonatal Diabetes International Collaborative Group; Hattersley AT, Ellard S. Edghill EL, et al. Among authors: kapoor rr. Diabetes. 2008 Apr;57(4):1034-42. doi: 10.2337/db07-1405. Epub 2007 Dec 27. Diabetes. 2008. PMID: 18162506 Free PMC article.
Hyperinsulinism in developmental syndromes.
Kapoor RR, James C, Hussain K. Kapoor RR, et al. Endocr Dev. 2009;14:95-113. doi: 10.1159/000207480. Epub 2009 Feb 27. Endocr Dev. 2009. PMID: 19293578 Review.
53 results