Mutations in HHEX are not a common cause of monogenic forms of beta cell dysfunction.
Κύριοι συγγραφείς: | Minton, J, van de Bunt, M, Boustred, C, Hussain, K, Hattersley, A, Ellard, S, Gloyn, A |
---|---|
Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
2007
|
Παρόμοια τεκμήρια
-
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.
ανά: Edghill, E, κ.ά.
Έκδοση: (2009) -
Monogenic disorders of the pancreatic β-cell: Personalizing treatment for rare forms of diabetes and hypoglycemia
ανά: van de Bunt, M, κ.ά.
Έκδοση: (2007) -
Defining the genetic aetiology of monogenic diabetes can improve treatment.
ανά: Gloyn, A, κ.ά.
Έκδοση: (2006) -
Monogenic β-cell dysfunction in children: Clinical phenotypes, genetic etiology and mutational pathways
ανά: Waterfield, T, κ.ά.
Έκδοση: (2008) -
Sequencing of candidate genes selected by beta cell experts in monogenic diabetes of unknown aetiology.
ανά: Edghill, E, κ.ά.
Έκδοση: (2010)