Genetic study of Alport syndrome in Tunisia
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00467-024-06474-7.pdf
Reference52 articles.
1. Savige J, Storey H, Watson E et al (2021) Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria. Eur J Hum Genet 29:1186–1197. https://doi.org/10.1038/s41431-021-00858-1
2. Nozu K, Nakanishi K, Abe Y 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
3. Warady BA, Agarwal R, Bangalore S et al (2020) Alport syndrome classification and management. Kidney Med 2:639–649. https://doi.org/10.1016/j.xkme.2020.05.014
4. Savige J, Renieri A, Ars E et al (2022) Digenic Alport syndrome. Clin J Am Soc Nephrol 17:1697–1706. https://doi.org/10.2215/CJN.03120322
5. Vos P, Zietse R, van Geel M, Brooks AS, Cransberg K (2018) Diagnosing Alport syndrome: lessons from the pediatric ward. Nephron 140:203–210. https://doi.org/10.1159/000492438
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