Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Disease Progression and NPHS1[original query] |
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Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome. Journal of the American Society of Nephrology : JASN 2010 Jul 21 (7): 1209-17. Machuca Eduardo, Benoit Geneviève, Nevo Fabien, Tête Marie-Josèphe, Gribouval Olivier, Pawtowski Audrey, Brandström Per, Loirat Chantal, Niaudet Patrick, Gubler Marie-Claire, Antignac Corin |
Association between genetic polymorphisms of the NPHS1 gene and membranous glomerulonephritis in the Taiwanese population. Clinica chimica acta; international journal of clinical chemistry 2010 May 411 (9-10): 714-8. Lo Wan-Yu, Chen Shih-Yin, Wang Huang-Joe, Shih Hung-Chang, Chen Cheng-Hsu, Tsai Chang-Hai, Tsai Fuu-J |
Case Report: A Pathogenic Missense Variant of WT1 Cosegregates With Proteinuria in a Six-Generation Chinese Family With IgA Nephropathy. Frontiers in medicine 2022 2 8 810940. Li Qianqian, Zhu Li, Shi Sufang, Xu Damin, Lv Jicheng, Zhang Ho |
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