Spectrum mutations of PRF1, UNC13D, STX11, and STXBP2 genes in Vietnamese patients with hemophagocytic lymphohistiocytosis

CONCLUSION: Vietnamese patients with HLH showed a distinct genetic variant spectrum, in which UNC13D is the predominant genetic lesion associated with HLH.PMID:34339548 | DOI:10.1111/ijlh.13674

Source: International Journal of Laboratory Hematology - August 2, 2021 Category: Hematology Authors: Phan Thi Xinh Ho Quoc Chuong Truong Pham Hong Diem Tuan Minh Nguyen Nguyen Dinh Van Nguyen Hoang Mai Anh Huynh Nghia Hoang Anh Vu Source Type: research