Citation to this article as recorded by
APOL1 risk genotype in European steroid-resistant nephrotic
syndrome and/or focal segmental glomerulosclerosis patients of different African
ancestries Nephrology Dialysis Transplantation |
A case report of congenital nephrotic syndrome caused by new mutations of NPHS1 Journal of International Medical Research Vol. 49, Issue 8, 030006052110381, 2021 |
How to cite this article
A.G. Behbahan, B. Poorshiri, F. Mortazavi, M.S. Khaniani and S.M. Derakhshan, 2013. NPHS1 Gene Mutations in Children with Nephrotic Syndrome in Northwest Iran. Pakistan Journal of Biological Sciences, 16: 882-886.
DOI: 10.3923/pjbs.2013.882.886
URL: https://scialert.net/abstract/?doi=pjbs.2013.882.886
DOI: 10.3923/pjbs.2013.882.886
URL: https://scialert.net/abstract/?doi=pjbs.2013.882.886