WHIM Syndrome-linked CXCR4 mutation alters cerebellar cytoarchitecture during early development triggering long-lasting behavioral defects

This dataset is part of a study by Demenego et al. and includes raw ex vivo anatomical MR images of Cxcr4^+/1013 knock-in mice, which serve as a model of Warts hypogammaglobulinemia immunodeficiency myelokathexis (WHIM) syndrome.

If you use this dataset in your work, please cite this article: Demenego G et al. [Neurodevelopmental origins of structural and psychomotor defects in CXCR4-linked primary immunodeficiency](https://doi.org/10.1016/j.neuron.2025.05.016). Neuron, 2025.