Associated Papers
CXCR2 deficiency with myelokathexis caused by a novel variant: correction via CRISPR/Cas9.
Hinke DM et al.
Haematologica, 2026
New genetic and epigenetic insights into the chemokine system: the latest discoveries aiding progression toward precision medicine.
Xu H et al.
Cellular & Molecular Immunology, 2023
Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity.
Marin-Esteban V et al.
Haematologica, 2022
34854278 (PubMed )
Supplement: 2021_279254_MARIN-ESTEBAN_SUPPL.pdf
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.
Auer PL et al.
Nature Genetics, 2014
Select a paper to view details