Author:
Ding Juanjuan,Liao Panli,Zhu Gaohong,Qi Chang,Liu Lili,Zhao Peiwei,Wang Xiaowen
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology and Child Health
Reference24 articles.
1. Habib R, Gubler MC, Hinglais N, Noel LH, Droz D, Levy M, Mahieu P, Foidart JM, Perrin D, Bois E, Grunfeld JP (1982) Alport’s syndrome: experience at Hopital Necker. Kidney Int Suppl 11:S20–S28
2. Kleppel MM, Kashtan CE, Butkowski RJ, Fish AJ, Michael AF (1987) Alport familial nephritis. Absence of 28 kilodalton non-collagenous monomers of type IV collagen in glomerular basement membrane. J Clin Invest 80:263–266. https://doi.org/10.1172/JCI113057
3. Feingold J, Bois E, Chompret A, Broyer M, Gubler MC, Grunfeld JP (1985) Genetic heterogeneity of Alport syndrome. Kidney Int 27:672–677. https://doi.org/10.1038/ki.1985.63
4. Beicht S, Strobl-Wildemann G, Rath S, Wachter O, Alberer M, Kaminsky E, Weber LT, Hinrichsen T, Klein HG, Hoefele J (2013) Next generation sequencing as a useful tool in the diagnostics of mosaicism in Alport syndrome. Gene 526:474–477. https://doi.org/10.1016/j.gene.2013.05.045
5. Ding Y, Tang X, Du Y, Chen H, Yu D, Zhu B, Yuan B (2021) Coexistence of Alport syndrome and C3 glomerulonephritis in a proband with family history. Eur J Med Res 26:71–75. https://doi.org/10.1186/s40001-021-00543-5
Cited by
1 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