Associated Papers
Determination of CD177 (human neutrophil antigen 2) polymorphisms using nanopore sequencing.
Kløve-Mogensen K et al.
Vox Sanguinis, 2025
Case Report: Multiple peripheral nerve demyelinating lesions and cerebrovascular injury which resulted in extensive cerebral infarction in a XLP1 patient without EBV infection.
Li J et al.
Frontiers in Immunology, 2025
40519929 (PubMed )
Supplement: Table2.xlsx › info_analysis
An accurate genetic assay to identify human neutrophil antigen 2 deficiency.
Li Y et al.
Transfusion Medicine (oxford, England), 2023
Whole exome sequencing with a focus on cardiac disease-associated genes in families of sudden unexplained deaths in Yunnan, southwest of China.
Wei SJ et al.
Bmc Genomics, 2023
36721086 (PubMed )
Supplement: 12864_2022_9097_MOESM2_ESM.xls › Sheet1
Human neutrophil antigen 2 sequence-based typing: Joining the hunt for the CD177 answer.
Browne T et al.
Vox Sanguinis, 2022
A novel nonsense mutation found in the CD177 gene of Thai individuals with the HNA-2 null phenotype.
Siriphanthong K et al.
Transfusion Medicine (oxford, England), 2020
Select a paper to view details