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Identification of the novel KIR3DL3*118 allele in a Chinese Han individual.

Jianxin ZhenZhi-Chao YangHao ChenZhi-Hui Deng
Published in: HLA (2023)
The novel KIR3DL3*118 allele differs from the closest allele KIR3DL3*01002 by a single missense mutation at CDS nt502 A > G in exon 4.
Keyphrases
  • quantum dots
  • intellectual disability
  • bioinformatics analysis