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Journal Article
Diabetes Research and Clinical Practice, ISSN 0168-8227, 2017, Volume 130, pp. 86 - 89
Highlights • We describe a novel GCK-MODY mutation in a Macedonian family, the very first family tested for GCK-MODY gene in the country. • To our knowledge,... 
Endocrinology & Metabolism | GCK mutation | Mild hyperglycemia | GCK-MODY | POPULATION | YOUNG | ENDOCRINOLOGY & METABOLISM | LINKAGE | Greece | Glucose Tolerance Test | Diabetes Mellitus, Type 2 - genetics | Humans | Diabetes Mellitus, Type 2 - therapy | Child, Preschool | Female | Glucokinase - genetics | Male | Mutation | Hyperglycemia - genetics | Hyperglycemia | Gene mutations | Isoenzymes | Genes
Journal Article
Journal of Pediatric Endocrinology and Metabolism, ISSN 0334-018X, 01/2017, Volume 30, Issue 1, pp. 97 - 100
Journal Article
Journal Article
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 2010, Volume 402, Issue 2, pp. 252 - 257
Journal Article
Journal Article
Journal Article
Molecular Medicine Reports, ISSN 1791-2997, 8/2015, Volume 12, Issue 2, pp. 2390 - 2394
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 06/2009, Volume 94, Issue 6, pp. 1959 - 1965
Context: Mutations in the HNF 1A gene are the most common cause of maturity-onset diabetes of the young (MODY) in most populations. India currently has the... 
INSULIN | I ALPHA-GENE | MODY | HNF-1-ALPHA | ENDOCRINOLOGY & METABOLISM | MUTATIONS | MELLITUS | PROMOTER | HEPATOCYTE-NUCLEAR-FACTOR-1-ALPHA | GCK | EPIDEMIOLOGY
Journal Article
Journal Article