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Mutations in HHEX are not a co...
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Mutations in HHEX are not a common cause of monogenic forms of beta cell dysfunction.
Manylion Llyfryddiaeth
Prif Awduron:
Minton, J
,
van de Bunt, M
,
Boustred, C
,
Hussain, K
,
Hattersley, A
,
Ellard, S
,
Gloyn, A
Fformat:
Journal article
Iaith:
English
Cyhoeddwyd:
2007
Daliadau
Disgrifiad
Eitemau Tebyg
Dangos Staff
Eitemau Tebyg
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.
gan: Edghill, E, et al.
Cyhoeddwyd: (2009)
Monogenic disorders of the pancreatic β-cell: Personalizing treatment for rare forms of diabetes and hypoglycemia
gan: van de Bunt, M, et al.
Cyhoeddwyd: (2007)
Defining the genetic aetiology of monogenic diabetes can improve treatment.
gan: Gloyn, A, et al.
Cyhoeddwyd: (2006)
Monogenic β-cell dysfunction in children: Clinical phenotypes, genetic etiology and mutational pathways
gan: Waterfield, T, et al.
Cyhoeddwyd: (2008)
Sequencing of candidate genes selected by beta cell experts in monogenic diabetes of unknown aetiology.
gan: Edghill, E, et al.
Cyhoeddwyd: (2010)