GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey

Haliloglu B., Hysenaj G., Atay Z., GÜRAN T., Abali S. , Turan S., ...Daha Fazla

CLINICAL ENDOCRINOLOGY, cilt.85, sa.3, ss.393-399, 2016 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 85 Konu: 3
  • Basım Tarihi: 2016
  • Doi Numarası: 10.1111/cen.13121
  • Sayfa Sayıları: ss.393-399


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.