Mutations in HHEX are not a common cause of monogenic forms of beta cell dysfunction.

Samankaltaisia teoksia

• Mutations in the third gene shown to alter fasting glucose levels in the population (G6PC2) are not a common cause of monogenic forms of pancreatic B-cell dysfunction.
  Tekijä: Edghill, E, et al.
  Julkaistu: (2009)
• Monogenic disorders of the pancreatic β-cell: Personalizing treatment for rare forms of diabetes and hypoglycemia
  Tekijä: van de Bunt, M, et al.
  Julkaistu: (2007)
• Defining the genetic aetiology of monogenic diabetes can improve treatment.
  Tekijä: Gloyn, A, et al.
  Julkaistu: (2006)
• Monogenic β-cell dysfunction in children: Clinical phenotypes, genetic etiology and mutational pathways
  Tekijä: Waterfield, T, et al.
  Julkaistu: (2008)
• Sequencing of candidate genes selected by beta cell experts in monogenic diabetes of unknown aetiology.
  Tekijä: Edghill, E, et al.
  Julkaistu: (2010)