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. 2023 Oct 16;109(3):e1204–e1224. doi: 10.1210/clinem/dgad606

Figure 2.

Figure 2.

Domain topology of the variants in LMNA and the association of the most common clinical phenotypes. FPLD2, familial partial lipodystrophy type 2; FSGS, focal segmental glomerulosclerosis.