Hereditary Proteinuric Glomerular Disorders
Author:
Publisher
Springer Singapore
Link
http://link.springer.com/content/pdf/10.1007/978-981-13-2977-7_21
Reference21 articles.
1. Barua M, Brown EJ, Charoonratana VT et al (2013) Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis. Kidney Int 83(2):316–322. https://doi.org/10.1038/ki.2012.349
2. Benoit G, Machuca E, Antignac C (2010) Hereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations. Pediatr Nephrol 25(9):1621–1632. https://doi.org/10.1007/s00467-010-1495-0
3. Boyer O, Nevo F, Plaisier E et al (2011) INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy. N Engl J Med 365(25):2377–2388. https://doi.org/10.1056/NEJMoa1109122
4. Breitsprecher D, Goode BL (2013) Formins at a glance. J Cell Sci 126:1–7. https://doi.org/10.1242/jcs.107250
5. Brown EJ, Schlondorff JS, Becker DJ et al (2010) Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42(1):72–76. https://doi.org/10.1038/ng.505
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