Genotype–phenotype correlations and response to glucose lowering therapy in subjects with HNF1β associated diabetes
Author:
Funder
health research board
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Internal Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00592-021-01794-8.pdf
Reference43 articles.
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2. Shepherd M, Shields B, Hammersley S, et al. (2016) United team systematic population screening, using biomarkers and genetic testing, identifies 25% of the UK pediatric diabetes population with monogenic diabetes. Diabetes Care. https://doi.org/10.2337/dc16-0645
3. Delvecchio M, Mozzillo E, Salzano G, et al. (2017) Diabetes Study Group of the Italian Society of Pediatric Endocrinology and Diabetes (ISPED). Monogenic Diabetes Accounts for 6.3% of Cases Referred to 15 Italian Pediatric Diabetes Centers During 2007 to 2012. J Clin Endocrinol Metab, https://doi.org/10.1210/jc.2016-2490.
4. Edghill EL, Stals K, Oram RA, et al (2013) HNF1B deletions in patients with young-onset diabetes but no known renal disease. Diabet Med 30(1):114–117. https://doi.org/10.1111/j.1464-5491.2012.03709.x
5. Kleinberger JW, Pollin TI (2015) Undiagnosed MODY: Time for Action. Curr DiabRep 15(12):110. https://doi.org/10.1007/s11892-015-0681-7
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