Author:
Li Guo-min,Xu Hong,Shen Qian,Gong Yi-nv,Fang Xiao-yan,Sun Li,Liu Hai-mei,An Yu
Publisher
Springer Science and Business Media LLC
Reference33 articles.
1. Cochat P, Hulton SA, Acquaviva C, Danpure CJ, Daudon M, De Marchi M, Fargue S, Groothoff J, Harambat J, Hoppe B, Jamieson NV, Kemper MJ, Mandrile G, Marangella M, Picca S, Rumsby G, Salido E, Straub M, van Woerden CS: Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment. Nephrol Dial Transplant. 2012, 27: 1729-1736.
2. Hoppe B: An update on primary hyperoxaluria. Nat Rev Nephrol. 2012, 8: 467-475.
3. Robbiano A, Mandrile G, De Marchi M, Beck B, Baasner A, Murer L, Benetti E, Giachino D: Novel human pathological mutations: Gene symbol: AGXT. Disease: hyperoxaluria. Hum Genet. 2010, 127: 468-
4. Cochat P, Rumsby G: Primary hyperoxaluria. N Engl J Med. 2013, 369: 649-658.
5. Latta K, Brodehl J: Primary hyperoxaluria type I. Eur J Pediatr. 1990, 149: 518-522.
Cited by
13 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献