HOGA1 variants in Chinese patients with primary hyperoxaluria type 3: genetic features and genotype–phenotype relationships
Author:
Publisher
Springer Science and Business Media LLC
Subject
Urology
Link
https://link.springer.com/content/pdf/10.1007/s00345-023-04461-5.pdf
Reference34 articles.
1. Williams EL, Bockenhauer D, van’t Hoff WG et al (2012) The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type 3. Nephrol Dial Transpl 27(8):3191–3195. https://doi.org/10.1093/ndt/gfs039
2. Belostotsky R, Pitt JJ, Frishberg Y (2012) Primary hyperoxaluria type III–a model for studying perturbations in glyoxylate metabolism. J Mol Med (Berlin) 90(12):1497–1504. https://doi.org/10.1007/s00109-012-0930-z
3. Monico CG, Rossetti S, Belostotsky R et al (2011) Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis. Clin J Am Soc Nephrol 6(9):2289–2295. https://doi.org/10.2215/cjn.02760311
4. Hoppe B (2012) An update on primary hyperoxaluria. Nat Rev Nephrol 8(8):467–475. https://doi.org/10.1038/nrneph.2012.113
5. Cochat P, Rumsby G (2013) Primary hyperoxaluria. N Engl J Med 369(7):649–658. https://doi.org/10.1056/NEJMra1301564
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