Variants in the isoform-specific coding regions of theHNF1A, HNF4AandHNF1Bgenes are not a common cause of familial, young-onset diabetes or renal cysts and diabetes (RCAD)
Author:
Publisher
Wiley
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1464-5491.2009.02705.x/fullpdf
Reference5 articles.
1. Alternate mRNA processing of the hepatocyte nuclear factor genes and its role in monogenic diabetes;Harries;Expert Rev Endocrinol Metab,2006
2. Clinical implications of a molecular genetic classification of monogenic β-cell diabetes;Murphy;Nat Clin Pract Endocrinol Metab,2008
3. The diabetic phenotype in HNF4A mutation carriers is moderated by the expression of HNF4A isoforms from the P1 promoter during fetal development;Harries;Diabetes,2008
4. Mutations in hepatocyte nuclear factor-1B and their related phenotypes;Edghill;J Med Genet,2006
5. More potent transcriptional activators or a transdominant inhibitor of the HNF1 homeoprotein family are generated by alternative RNA processing;Bach;EMBO J,1993
Cited by 2 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
1. MODY3, renal cysts, and Dandy-Walker variants with a microdeletion spanning the HNF1A gene;Clinical Nephrology;2017-09-01
2. Genetic kidney diseases;The Lancet;2010-04
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