Unveiling the genetic architecture of kidney disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
http://www.nature.com/articles/nrneph.2017.177.pdf
Reference10 articles.
1. Devuyst, O., Knoers, N. V., Remuzzi, G. & Schaefer, F. Rare inherited kidney diseases: challenges, opportunities, and perspectives. Lancet 383, 1844–1859 (2014).
2. Wuttke, M. & Köttgen, A. Insights into kidney diseases from genome-wide association studies. Nat. Rev. Nephrol. 12, 549–562 (2016).
3. Sadowski, C. E. et al. A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome. J. Am. Soc. Nephrol. 26, 1279–1289 (2015).
4. Lovric, S. et al. Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency. J. Clin. Invest. 127, 912–928 (2017).
5. Prasad, R. et al. Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome. J. Clin. Invest. 127, 942–953 (2017).
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