A young Chinese gentleman with GCK-MODY
Case Report
DOI:
https://doi.org/10.58372/2835-6276.1415Abstract
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References
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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(7):1383-1392.
Rudland VL. Diagnosis and management of glucokinase monogenic diabetes in pregnancy: current perspectives. Diabetes Metab Syndr Obes. 2019;12:1081-1089.
Hulín J, Škopková M, Valkovičová T, et al. Clinical implications of the glucokinase impaired function - GCK MODY today. Physiol Res. 2020;69(6):995-1011.
Ellard S, Bellanne-Chantelot C, Hattersley AT, European Molecular Genetics Quality Network MODY group. Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young. Diabetologia 2008;51: 546-553.
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