Fol. Biol. 2012, 58, 64-68
https://doi.org/10.14712/fb2012058020064
Mutational Analysis of the NPHS2 Gene in Czech Patients with Idiopathic Nephrotic Syndrome
Jana Reiterová1,2, H. Šafránková
1, L. Obeidová
2, J. Štekrová
1,2, D. Maixnerová
1, M. Merta
2,3, V. Tesař
1
1Department of Nephrology, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic
2Institute of Biology and Human Genetics, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic
3Department of Metabolic Care and Gerontology, University Hospital in Hradec Králové, Charles University in Prague, Hradec Králové, Czech Republic
Received October 2011
Accepted January 2012
Crossref Cited-by Linking
- Zhou Qiongxiu, Weng Qinjie, Zhang Xiaoyan, Liu Yunzi, Tong Jun, Hao Xu, Shi Hao, Shen Pingyan, Ren Hong, Xie Jingyuan, Chen Nan: Association Between NPHS2 p.R229Q and Focal Segmental Glomerular Sclerosis/Steroid-Resistant Nephrotic Syndrome. Front. Med. 2022, 9. <https://doi.org/10.3389/fmed.2022.937122>