Author:
Shields B. M.,Hicks S.,Shepherd M. H.,Colclough K.,Hattersley A. T.,Ellard S.
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology, Diabetes and Metabolism,Internal Medicine
Reference12 articles.
1. Tattersall RB (1974) Mild familial diabetes with dominant inheritance. Q J Med 43:339–357
2. Shepherd M, Shields B, Ellard S, Rubio-Cabezas O, Hattersley AT (2009) A genetic diagnosis of HNF1A diabetes alters treatment and improves glycaemic control in the majority of insulin-treated patients. Diabet Med 26:437–441
3. Estalella I, Rica I, Perez de Nanclares G et al (2007) Mutations in GCK and HNF-1alpha explain the majority of cases with clinical diagnosis of MODY in Spain. Clin Endocrinol (Oxf) 67:538–546
4. Chevre JC, Hani EH, Boutin P et al (1998) Mutation screening in 18 Caucasian families suggest the existence of other MODY genes. Diabetologia 41:1017–1023
5. Murphy R, Ellard S, Hattersley AT (2008) Clinical implications of a molecular genetic classification of monogenic beta-cell diabetes. Nat Clin Pract Endocrinol Metab 4:200–213
Cited by
559 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献