Monogenic diabetes
Author:
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s13340-024-00698-6.pdf
Reference37 articles.
1. Hashimoto Y, Dateki S, Hirose M, et al. Molecular and clinical features of KATP -channel neonatal diabetes mellitus in Japan. Pediatr Diabetes. 2017;18:532–9.
2. Horikawa Y. Maturity-onset diabetes of the young (MODY) as a model for elucidating the multifactorial origin of type 2 diabetes mellitus. J Diabetes Investig. 2018;9:704–12.
3. Chakera AJ, Steele AM, Gloyn AL, et al. Recognition and management of individuals with hyperglycemia because of a heterozygous glucokinase mutation. Diabetes Care. 2015;38:1383–92.
4. Hattersley AT, Beards F, Ballantyne E, et al. Mutations in the glucokinase gene of the fetus result in reduced birth weight. Nat Genet. 1998;19:268–70.
5. Steele AM, Shields BM, Wensley KJ, et al. Prevalence of vascular complications among patients with glucokinase mutations and prolonged, mild hyperglycemia. JAMA. 2014;311:279–86.
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