We observed an enrichment of megakaryocytes, CD16+ monocytes, CD8+ Temra (terminally differentiated effector), CD4+ Tcm (central memory), and CD56+ MM in the TME, as well as a decrease of plasmacytoid DCs (pDCs), immature granulocytes, and CD27+ normal plasma cells (NPC) (Fig. 2b). The gene discussed is NCAM1; the disease is Miyoshi myopathy.