FIGURE 7.3, Mutations in the Glucokinase Gene Reduce Glucose Phosphorylating Capacity and Result in Diabetes - Diabetes in America - NCBI Bookshelf
Glucokinase (GCK) Mutations and Their Characterization in MODY2 Children of Southern Italy | PLOS ONE
MODY2 in Asia: analysis of GCK mutations and clinical characteristics in: Endocrine Connections Volume 9 Issue 5 (2020)
Maturity onset diabetes of the young type 2 (MODY2): Insight from an extended family - Diabetes Research and Clinical Practice
MODY: A Rare Type of Diabetes - Clinical Advisor
Genetic and clinical characteristics of maturity-onset diabetes of the young in Chinese patients | European Journal of Human Genetics
Serum glucose and insulin concentrations during the OGTT in MODY2... | Download Scientific Diagram
Identification of Candidate Children for Maturity-Onset Diabetes of the Young Type 2 (MODY2) Gene Testing: A Seven-Item Clinical Flowchart (7-iF) | PLOS ONE
Endocrines | Free Full-Text | Maturity-Onset Diabetes of the Young (MODY): Genetic Causes, Clinical Characteristics, Considerations for Testing, and Treatment Options
Molecular Mechanisms and Clinical Pathophysiology of Maturity-Onset Diabetes of the Young | NEJM
Mutations in GCK May Lead to MODY2 by Reducing Glycogen Synthesis - Li - 2022 - Advanced Biology - Wiley Online Library
Using Clinical Indices to Distinguish MODY2 (GCK Mutation) and MODY3 (HNF1A Mutation) from Type 1 Diabetes in a Young Chinese Population | SpringerLink
Mutations in the MODY3 and MODY2 genes | Download Table
Biochemical characterization of novel glucokinase mutations isolated from Spanish maturity-onset diabetes of the young (MODY2) patients | Journal of Human Genetics
A Type of Diabetes Called MODY2!
Frontiers | Genetic Testing of Maturity-Onset Diabetes of the Young Current Status and Future Perspectives
Final Diagnosis -- Case 634
Prevalence of MODY2 and MODY3 in different countries. | Download Table
PDF) MUTATIONS IN THE GCK GENE PROMOTER MAY BE RESPONSIBLE FOR MODY2 DISEASE | IJMRPS Journal - Academia.edu
Clinical assessment of HNF1A and GCK variants and identification of a novel mutation causing MODY2
