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Available from: https:\/\/franklin.genoox.com\/clinical-db\/home"},{"key":"9","unstructured":"9. Varsome [Internet]. [cited 2023 May 25]. Available from: https:\/\/varsome.com\/"},{"key":"10","unstructured":"10. Committee for the Revision of the Clinical Guide for Atypical Hemolytic Uremic Syndrome. Clinical Guide for Atypical Hemolytic Uremic Syndrome 2023. Tokyo-Igakusha, Tokyo, 2023 (in Japanese)."},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Noris M, Remuzzi G. Genetics of immune-mediated glomerular diseases: focus on complement. Semin Nephrol 37: 447-463, 2017.","DOI":"10.1016\/j.semnephrol.2017.05.018"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Osborne AJ, Breno M, Borsa NG, et al. Statistical validation of rare complement variants provides insights into the molecular basis of atypical hemolytic uremic syndrome and C3 glomerulopathy. 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[cited 2023 May 24]. Available from: https:\/\/jmorp.megabank.tohoku.ac.jp\/"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Noris M, Caprioli J, Bresin E, et al. Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype. Clin J Am Soc Nephrol 5: 1844-1859, 2010.","DOI":"10.2215\/CJN.02210310"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Fremeaux-Bacchi V, Fakhouri F, Garnier A, et al. Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults. Clin J Am Soc Nephrol 8: 554-562, 2013.","DOI":"10.2215\/CJN.04760512"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19. Maga TK, Nishimura CJ, Weaver AE, Frees KL, Smith RJH. Mutation in alternative pathway complement proteins in American patients with atypical hemolytic syndrome. 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