Utility of genetic screening in children with nephrotic syndrome presenting during the first year of life
- PMID: 17622228
- DOI: 10.1038/ncpneph0560
Utility of genetic screening in children with nephrotic syndrome presenting during the first year of life
Comment on
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Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).Pediatrics. 2007 Apr;119(4):e907-19. doi: 10.1542/peds.2006-2164. Epub 2007 Mar 19. Pediatrics. 2007. PMID: 17371932
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