Browsing 2016 RD&E publications by Subject "Base Sequence"
Now showing items 1-1 of 1
GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey. (Wiley, 2016-09)Inactivating 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 ...