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Genotype-phenotype correlation of X-linked Alport syndrome observed in both genders: a multicenter study in South Korea.
Kim JH, Lim SH, Song JY, Cho MH, Hyun H, Yang EM, Lee JW, Cho MH, Park MJ, Lee JH, Jung J, Yoo KH, Jang KM, Pai KS, Suh JS, Namgoong MK, Chung WY, Kim SJ, Cho EY, Kim KM, Kim NH, Kim M, Paik JH, Kang HG, Ahn YH, Cheong HI. Kim JH, et al. Among authors: lee jw, lee jh. Sci Rep. 2023 Apr 26;13(1):6827. doi: 10.1038/s41598-023-34053-7. Sci Rep. 2023. PMID: 37100867 Free PMC article.
Phenotype and genotype of Dent's disease in three Korean boys.
Cheong HI, Lee JW, Zheng SH, Lee JH, Kang JH, Kang HG, Ha IS, Lee SJ, Choi Y. Cheong HI, et al. Among authors: lee sj, lee jw, lee jh. Pediatr Nephrol. 2005 Apr;20(4):455-9. doi: 10.1007/s00467-004-1769-5. Epub 2005 Feb 18. Pediatr Nephrol. 2005. PMID: 15719255
Mutational analysis of idiopathic renal hypouricemia in Korea.
Cheong HI, Kang JH, Lee JH, Ha IS, Kim S, Komoda F, Sekine T, Igarashi T, Choi Y. Cheong HI, et al. Among authors: lee jh. Pediatr Nephrol. 2005 Jul;20(7):886-90. doi: 10.1007/s00467-005-1863-3. Epub 2005 May 24. Pediatr Nephrol. 2005. PMID: 15912381
Renal manifestations of patients with MYH9-related disorders.
Han KH, Lee H, Kang HG, Moon KC, Lee JH, Park YS, Ha IS, Ahn HS, Choi Y, Cheong HI. Han KH, et al. Among authors: lee h, lee jh. Pediatr Nephrol. 2011 Apr;26(4):549-55. doi: 10.1007/s00467-010-1735-3. Epub 2011 Jan 6. Pediatr Nephrol. 2011. PMID: 21210153
Genetic basis of Bartter syndrome in Korea.
Lee BH, Cho HY, Lee H, Han KH, Kang HG, Ha IS, Lee JH, Park YS, Shin JI, Lee DY, Kim SY, Choi Y, Cheong HI. Lee BH, et al. Among authors: lee dy, lee h, lee jh. Nephrol Dial Transplant. 2012 Apr;27(4):1516-21. doi: 10.1093/ndt/gfr475. Epub 2011 Aug 23. Nephrol Dial Transplant. 2012. PMID: 21865213
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