Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia.

অনুরূপ উপাদানগুলি

• Glucokinase (GCK) mutations in hyper- and hypoglycemia: maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy.
  অনুযায়ী: Gloyn, A
  প্রকাশিত: (2003)
• Identification of 21 novel glucokinase (GCK) mutations in UK and European Caucasians with maturity-onset diabetes of the young (MODY).
  অনুযায়ী: Thomson, K, অন্যান্য
  প্রকাশিত: (2003)
• Discovery of a novel site regulating glucokinase activity following characterization of a new mutation causing hyperinsulinemic hypoglycemia in humans.
  অনুযায়ী: Beer, N, অন্যান্য
  প্রকাশিত: (2011)
• Permanent neonatal diabetes mellitus caused by a novel homozygous (T168A) glucokinase (GCK) mutation: initial response to oral sulphonylurea therapy.
  অনুযায়ী: Turkkahraman, D, অন্যান্য
  প্রকাশিত: (2008)
• Persistent hyperinsulinemic hypoglycemia in a 7 yr old girl due to a novel activating glucokinase mutation
  অনুযায়ী: Lahr, G, অন্যান্য
  প্রকাশিত: (2007)