CLINICAL ENDOCRINOLOGY, cilt.85, sa.3, ss.393-399, 2016 (SCI-Expanded)
ObjectiveInactivating heterozygous mutations in the GCK gene are a common cause of MODY and result in mild fasting hyperglycaemia, which does not require treatment. We aimed to identify the frequency, clinical and molecular features of GCK mutations in a Turkish paediatric cohort.