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

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

Detalles Bibliográficos
Main Authors: van de Bunt, M, Edghill, E, Hussain, K, Ellard, S, Gloyn, A
Formato: Journal article
Idioma:English
Publicado: 2008
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Descripción
Summary:

Títulos similares

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

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