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

Ítems similars

• 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.
  per: Edghill, E, et al.
  Publicat: (2009)
• Monogenic disorders of the pancreatic β-cell: Personalizing treatment for rare forms of diabetes and hypoglycemia
  per: van de Bunt, M, et al.
  Publicat: (2007)
• Defining the genetic aetiology of monogenic diabetes can improve treatment.
  per: Gloyn, A, et al.
  Publicat: (2006)
• Monogenic β-cell dysfunction in children: Clinical phenotypes, genetic etiology and mutational pathways
  per: Waterfield, T, et al.
  Publicat: (2008)
• Sequencing of candidate genes selected by beta cell experts in monogenic diabetes of unknown aetiology.
  per: Edghill, E, et al.
  Publicat: (2010)