Trimerization profile of type IV collagen COL4A5 exon deletion in X-linked Alport syndrome
Author:
Funder
Japan Society for the Promotion of Science
Japan Agency for Medical Research and Development
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s10157-024-02503-9.pdf
Reference30 articles.
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2. Nozu K, Nakanishi K, Abe Y, Udagawa T, Okada S, Okamoto T, et al. A review of clinical characteristics and genetic backgrounds in Alport syndrome. Clin Exp Nephrol. 2019;23:158–68.
3. Miner JH. Glomerular basement membrane composition and the filtration barrier. Pediatr Nephrol. 2011;26:1413–7.
4. Chew C, Lennon R. Basement membrane defects in genetic kidney diseases. Front Pediatr. 2018;6:11.
5. Kashtan CE, Ding J, Garosi G, Heidet L, Massella L, Nakanishi K, et al. Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the alport syndrome classification working group. Kidney Int. 2018;93:1045–51.
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