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    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 lymphohistiocytosis by HOI SOO YOON, KIM, Hee-Jin, BAE, Keun-Wook, LEE, Ki-O, SHIN, Ji-Sook, LEE, Seung-Tae, CHUNG, Hae-Sun, KIM, Sun-Hee, PARK, Chan-Jeoung, CHI, Hyun-Sook, IM, Ho-Joon, JONG JIN SEO, YOO, Keon-Hee, SUNG, Ki-Woong, KOO, Hong-Hoe, HYOUNG JIN KANG, HEE YOUNG SHIN, HYO SEOP ANN, KIM, Ji-Yoon, LIM, Young-Tak

    Published in Haematologica (Roma)
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