Associated Papers
CXCR2 deficiency with myelokathexis caused by a novel variant: correction via CRISPR/Cas9.
Hinke DM et al.
Haematologica, 2026
Expanding the genetic landscape of congenital neutropenia: CXCR2 mutations in three families revealed through whole exome sequencing.
Klimiankou M et al.
Haematologica, 2024
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
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.
Auer PL et al.
Nature Genetics, 2014
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