![UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis]()
UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosisYoon, H. S.; Kim, H. J.; Yoo, K. H.; Sung, K. W.; Koo, H. H.; Kang, H. J.; Shin, H. Y.; Ahn, H. S.; Kim, J. Y.; Lim, Y. T.; Bae, K. W.; Lee, K. O.; Shin, J. S.; Lee, S. T.; Chung, H. S.; Kim, S. H.; Park, C. J.; Chi, H. S.; Im, H. J.; Seo, J. J. · Haematologica · 2010