Copyright
©The Author(s) 2015.
World J Nephrol. May 6, 2015; 4(2): 235-244
Published online May 6, 2015. doi: 10.5527/wjn.v4.i2.235
Published online May 6, 2015. doi: 10.5527/wjn.v4.i2.235
Resource | Web address |
Oxalosis and Hyperoxaluria Foundation | http://www.ohf.org/ |
Rare Disease Initiative of the Renal Association | http://rarerenal.org/ |
Rare Diseases Clinical Research Network (links to the Rare Kidney Stone Consortium) | http://www.rarediseasesnetwork.org/ |
Children Living with Inherited Metabolic Diseases | http://www.climb.org.uk/ |
Genetics Home Reference | http://ghr.nlm.nih.gov/ |
Office of Rare Diseases Research | http://rarediseases.info.nih.gov/ |
National Organization for Rare Disorders | http://www.rarediseases.org/ |
- Citation: Bhasin B, Ürekli HM, Atta MG. Primary and secondary hyperoxaluria: Understanding the enigma. World J Nephrol 2015; 4(2): 235-244
- URL: https://www.wjgnet.com/2220-6124/full/v4/i2/235.htm
- DOI: https://dx.doi.org/10.5527/wjn.v4.i2.235