HNF1Bdeletions in patients with young-onset diabetes but no known renal disease

Author:

Edghill E. L.,Stals K.,Oram R. A.,Shepherd M. H.,Hattersley A. T.,Ellard S.

Publisher

Wiley

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference17 articles.

1. Mutation in hepatocyte nuclear factor-1β gene (TCF2) associated with MODY;Horikawa;Nat Genet,1997

2. Systematic review of TCF2 anomalies in renal cysts and diabetes syndrome/maturity onset diabetes of the young type 5;Chen;Chinese Med J,2010

3. Large genomic rearrangements in the hepatocyte nuclear factor-1beta (TCF2) gene are the most frequent cause of maturity-onset diabetes of the young type 5;Bellanne-Chantelot;Diabetes,2005

4. Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy;Mefford;Am J Hum Genet,2007

5. Hepatocyte nuclear factor-1β gene deletions are common in subjects with unexplained renal disease and diabetes;Edghill;Diabet Med,2006

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