Clinical, histological and molecular characteristics of Alport syndrome in Chinese children
Author:
Funder
Key R&D Program of Science & Technology of Hubei Province
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
https://link.springer.com/content/pdf/10.1007/s40620-023-01570-7.pdf
Reference36 articles.
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2. McCoy RC, Johnson HK, Stone WJ, Wilson CB (1982) Absence of nephritogenic gbm antigen(s) in some patients with hereditary nephritis. Kidney Int 21:642–652. https://doi.org/10.1038/ki.1982.72
3. Horinouchi T, Yamamura T, Minamikawa S, Nagano C, Sakakibara N, Nakanishi K et al (2020) Pathogenic evaluation of synonymous col4a5 variants in x-linked Alport syndrome using a minigene assay. Mol Genet Genomic Med 8:e1342. https://doi.org/10.1002/mgg3.1342
4. Kruegel J, Rubel D, Gross O (2013) Alport syndrome–insights from basic and clinical research. Nat Rev Nephrol 9:170–178. https://doi.org/10.1038/nrneph.2012.259
5. Nozu K, Nakanishi K, Abe Y, Udagawa T, Okada S, Okamoto T et al (2019) A review of clinical characteristics and genetic backgrounds in Alport syndrome. Clin Exp Nephrol 23:158–168. https://doi.org/10.1007/s10157-018-1629-4
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