1. Kashtan, Clifford E. 2020. Alport Syndrome: Achieving Early Diagnosis and Treatment. In American journal of kidney diseases : the official journal of the National Kidney Foundation, 77, 272-279. doi:10.1053/j.ajkd.2020.03.026. https://pubmed.ncbi.nlm.nih.gov/32712016/
2. Yari, Davood, Ehsanbakhsh, Zohreh, Validad, Mohammad-Hosein, Langroudi, Farzaneh Hasanian. 2020. Association of TIMP-1 and COL4A4 Gene Polymorphisms with Keratoconus in an Iranian Population. In Journal of ophthalmic & vision research, 15, 299-307. doi:10.18502/jovr.v15i3.7448. https://pubmed.ncbi.nlm.nih.gov/32864060/
3. Savige, Judy, Lipska-Zietkiewicz, Beata S, Watson, Elizabeth, Storey, Helen, Flinter, Frances. 2021. Guidelines for Genetic Testing and Management of Alport Syndrome. In Clinical journal of the American Society of Nephrology : CJASN, 17, 143-154. doi:10.2215/CJN.04230321. https://pubmed.ncbi.nlm.nih.gov/34930753/
4. Savige, Judy, Renieri, Alessandra, Ars, Elisabet, Lipska-Zietkiewicz, Beata, Gibson, Joel T. 2022. Digenic Alport Syndrome. In Clinical journal of the American Society of Nephrology : CJASN, 17, 1697-1706. doi:10.2215/CJN.03120322. https://pubmed.ncbi.nlm.nih.gov/35675912/
5. 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/
6. Imafuku, Aya, Nozu, Kandai, Sawa, Naoki, Nakanishi, Koichi, Ubara, Yoshifumi. 2020. How to resolve confusion in the clinical setting for the diagnosis of heterozygous COL4A3 or COL4A4 gene variants? Discussion and suggestions from nephrologists. In Clinical and experimental nephrology, 24, 651-656. doi:10.1007/s10157-020-01880-1. https://pubmed.ncbi.nlm.nih.gov/32232700/
7. Storey, Helen, Savige, Judy, Sivakumar, Vanessa, Abbs, Stephen, Flinter, Frances A. 2013. COL4A3/COL4A4 mutations and features in individuals with autosomal recessive Alport syndrome. In Journal of the American Society of Nephrology : JASN, 24, 1945-54. doi:10.1681/ASN.2012100985. https://pubmed.ncbi.nlm.nih.gov/24052634/
智鼠故事 
