Complete glucokinase deficiency is not a common cause of permanent neonatal diabetes.

Ítems similars

• Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood.
  per: Flanagan, SE, et al.
  Publicat: (2007)
• Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood (vol 56, pg 1930, 2007)
  per: Flanagan, SE, et al.
  Publicat: (2008)
• Permanent neonatal diabetes in an Asian infant.
  per: Porter, JR, et al.
  Publicat: (2005)
• Erratum: Mutations in ATP-sensitive K+ cannel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood (Diabetes (2007) 56 (1930-1937))
  per: Flanagan, SE, et al.
  Publicat: (2008)
• Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia.
  per: Osbak, K, et al.
  Publicat: (2009)