Gene duplications resulting in over expression of glucokinase are not a common cause of hypoglycaemia of infancy in humans.

Παρόμοια τεκμήρια

• Phenotypic heterogeneity in a family with a novel activating glucokinase (GCK) mutation (G68V) causing familial persistent hyperinsulinaemic hypoglycaemia of infancy
  ανά: Gloyn, A, κ.ά.
  Έκδοση: (2007)
• Familial persistent hyperinsulinaemic hypoglycaemia of infancy due to a novel glucokinase (GCK) activating mutation G68V
  ανά: Gloyn, A, κ.ά.
  Έκδοση: (2006)
• Insights into biochemical and genetical basis of glucokinase activation from naturally occuring hypoglycaemia mutations
  ανά: Gloyn, A, κ.ά.
  Έκδοση: (2003)
• Complete glucokinase deficiency is not a common cause of permanent neonatal diabetes.
  ανά: Gloyn, A, κ.ά.
  Έκδοση: (2002)
• Heterogeneity in disease severity in a family with a novel G68V GCK activating mutation causing persistent hyperinsulinaemic hypoglycaemia of infancy.
  ανά: Wabitsch, M, κ.ά.
  Έκδοση: (2007)