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UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis.
Yoon HS, Kim HJ, Yoo KH, Sung KW, Koo HH, Kang HJ, Shin HY, Ahn HS, Kim JY, Lim YT, Bae KW, Lee KO, Shin JS, Lee ST, Chung HS, Kim SH, Park CJ, Chi HS, Im HJ, Seo JJ. Yoon HS, et al. Among authors: lee ko, lee st. Haematologica. 2010 Apr;95(4):622-6. doi: 10.3324/haematol.2009.016949. Epub 2009 Dec 16. Haematologica. 2010. PMID: 20015888 Free PMC article.
Molecular detection of tyrosine hydroxylase in the peripheral blood of patients with neuroblastoma: useful at diagnosis but not predictive of subsequent relapse during off-therapy follow-up.
Lee ST, Ki CS, Sung KW, Kim HJ, Kim JW, Kim SH, Lee SH, Yoo KH, Koo HH, Kim JY, Cho EJ. Lee ST, et al. Among authors: lee sh. Pediatr Hematol Oncol. 2011 Feb;28(1):16-23. doi: 10.3109/08880018.2010.514694. Epub 2010 Nov 17. Pediatr Hematol Oncol. 2011. PMID: 21083359
2,370 results