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

Phan Thi XinhHo Quoc ChuongTruong Pham Hong DiemTuan Minh NguyenNguyen Dinh VanNguyen Hoang Mai AnhHuynh NghiaHoang Anh Vu
Published in: International journal of laboratory hematology (2021)
Vietnamese patients with HLH showed a distinct genetic variant spectrum, in which UNC13D is the predominant genetic lesion associated with HLH.
Keyphrases
  • genome wide
  • copy number
  • dna methylation
  • gene expression
  • transcription factor