NOS3 tagSNPs does not modify the chronic kidney disease progression in autosomal dominant polycystic kidney disease
Author:
Affiliation:
1. Department of Biomedical Sciences; Sri Ramachandra University; Chennai India
2. Department of Nephrology; Sri Ramachandra University; Chennai India
3. Sickle Cell Institute Chhattisgarh; Raipur India
Funder
Sri Ramachandra University, Chennai
Publisher
Wiley
Subject
Nephrology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/nep.12278/fullpdf
Reference31 articles.
1. Family history of renal disease severity predicts the mutated gene in ADPKD;Barua;J. Am. Soc. Nephrol.,2009
2. Diagnostic approach in autosomal dominant polycystic kidney disease;Pei;Clin. J. Am. Soc. Nephrol.,2006
3. The position of the polycystic kidney disease 1 (PKD1) gene mutation correlates with the severity of renal disease;Rossetti;J. Am. Soc. Nephrol.,2002
4. The role of parental hypertension in the frequency and age of diagnosis of hypertension in offspring with autosomal-dominant polycystic kidney disease;Schrier;Kidney Int.,2003
5. Endothelial nitric oxide synthase gene variant modulates the relationship between serum cholesterol levels and blood pressure in the general population: New evidence for a direct effect of lipids in arterial blood pressure;Pereira;Atherosclerosis,2006
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