Similarly, in Duchenne muscular dystrophy (DMD) mouse models, integrated Visium spatial and single‐cell transcriptomics revealed FAP expansion and CCC networks emanating from dystrophic regions, with distinct inflammatory (Ccl2, Ccl7, and Spp1) and regenerative‐like enriched collagen expressing FAPs clusters [21]. The gene discussed is CCL2; the disease is Duchenne muscular dystrophy.