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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: im hj. Haematologica. 2010 Apr;95(4):622-6. doi: 10.3324/haematol.2009.016949. Epub 2009 Dec 16. Haematologica. 2010. PMID: 20015888 Free PMC article.
Role of p16 in the pathogenesis of Langerhans cell histiocytosis.
Kim SY, Kim HJ, Kim HJ, Park MR, Koh KN, Im HJ, Lee CH, Seo JJ. Kim SY, et al. Among authors: im hj. Korean J Hematol. 2010 Dec;45(4):247-52. doi: 10.5045/kjh.2010.45.4.247. Epub 2010 Dec 31. Korean J Hematol. 2010. PMID: 21253426 Free PMC article.
467 results