Associated Papers
MODY2 in Asia: analysis of GCK mutations and clinical characteristics.
Zhou Y et al.
Endocrine Connections, 2020
Targeted next generation sequencing in patients with maturity-onset diabetes of the young (MODY).
Özdemir TR et al.
Journal of Pediatric Endocrinology & Metabolism : Jpem, 2018
GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey.
Haliloglu B et al.
Clinical Endocrinology, 2016
A novel glucokinase gene mutation and its effect on glycemic/C-peptide fluctuations in a patient with maturity-onset diabetes of the young type 2.
Loomba-Albrecht LA et al.
Diabetes Research and Clinical Practice, 2010
Mutations in GCK and HNF-1alpha explain the majority of cases with clinical diagnosis of MODY in Spain.
Estalella I et al.
Clinical Endocrinology, 2007
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