FRMD3 in diabetic nephropathy—guilt by association
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
http://www.nature.com/articles/nrneph.2013.81.pdf
Reference10 articles.
1. Martini, S. et al. From SNP to transcriptional mechanism: a model for FRMD3 in diabetic nephropathy. Diabetes http://dx.doi.org/10.2337/db12–1416 .
2. Bowden, D. W. & Freedman, B. I. The challenging search for diabetic nephropathy genes. Diabetes 61, 1923–1924 (2012).
3. Freedman, B. I. et al. Differential effects of MYH9 and APOL1 risk variants on FRMD3 association with diabetic ESRD in African Americans. PLoS Genet. 7, e1002150 (2011).
4. Hu, C. et al. CPVL/CHN2 genetic variant is associated with diabetic retinopathy in Chinese type 2 diabetic patients. Diabetes 60, 3085–3089 (2011).
5. Maeda, S. et al. Replication study for the association between four loci identified by a genome-wide association study on European American subjects with type 1 diabetes and susceptibility to diabetic nephropathy in Japanese subjects with type 2 diabetes. Diabetes 59, 2075–2079 (2010).
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