1. Yuan, Xiaohan, Su, Qing, Wang, Hui, Zhu, Li, Zhang, Hong. 2022. Genetic Variants of the COL4A3 , COL4A4 , and COL4A5 Genes Contribute to Thinned Glomerular Basement Membrane Lesions in Sporadic IgA Nephropathy Patients. In Journal of the American Society of Nephrology : JASN, 34, 132-144. doi:10.1681/ASN.2021111447. https://pubmed.ncbi.nlm.nih.gov/36130833/
2. Bekheirnia, Mir Reza, Reed, Berenice, Gregory, Martin C, Masoumi, Amirali, Schrier, Robert W. 2010. Genotype-phenotype correlation in X-linked Alport syndrome. In Journal of the American Society of Nephrology : JASN, 21, 876-83. doi:10.1681/ASN.2009070784. https://pubmed.ncbi.nlm.nih.gov/20378821/
3. De Silva, Samantha R, Arno, Gavin, Robson, Anthony G, Webster, Andrew R, Mahroo, Omar A. 2020. The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies. In Progress in retinal and eye research, 82, 100898. doi:10.1016/j.preteyeres.2020.100898. https://pubmed.ncbi.nlm.nih.gov/32860923/
4. Gregorio, Vanessa De, Caparali, Emine Bilge, Shojaei, Azadeh, Ricardo, Samantha, Barua, Moumita. 2023. Alport Syndrome: Clinical Spectrum and Therapeutic Advances. In Kidney medicine, 5, 100631. doi:10.1016/j.xkme.2023.100631. https://pubmed.ncbi.nlm.nih.gov/37122389/
5. Savige, Judy, Ariani, Francesca, Mari, Francesca, Garosi, Guido, Storey, Helen. 2018. Expert consensus guidelines for the genetic diagnosis of Alport syndrome. In Pediatric nephrology (Berlin, Germany), 34, 1175-1189. doi:10.1007/s00467-018-3985-4. https://pubmed.ncbi.nlm.nih.gov/29987460/
6. Bruni, V, Petrisano, M, Tarsitano, F, Chimenz, R, Concolino, D. . Alport's syndrome. In Journal of biological regulators and homeostatic agents, 33, 19-24. Special Issue: Focus on Pediatric Nephrology. doi:. https://pubmed.ncbi.nlm.nih.gov/31630709/
智鼠故事 
