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

Benzer Materyaller

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