Author:
Asfahani Rowan I.,Tahoun Mona M.,Miller-Hodges Eve V.,Bellerby Jack,Virasami Alex K.,Sampson Robert D.,Moulding Dale,Sebire Neil J.,Hohenstein Peter,Scambler Peter J.,Waters Aoife M.
Reference48 articles.
1. US Renal Data System 2015 Annual Data Report: Epidemiology of Kidney Disease in the United States;Saran;Am J Kidney Dis,2016
2. LMX1B mutations cause hereditary FSGS without extrarenal involvement;Boyer;J Am Soc Nephrol,2013
3. The genetics of nephrotic syndrome;Rheault;J Pediatr Genet,2016
4. WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis;Denamur;Kidney Int,2000
5. Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations;Chernin;Clin J Am Soc Nephrol,2010
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