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. 2025 May 29;110(11):2819–2822. doi: 10.3324/haematol.2025.287393

Figure 2.

Figure 2.

Six-generation pedigree of a family with hereditary myopathy, lactic acidosis and sideroblastic anemia syndrome type 1 (MLASA1). Squares represent males and circles females; diamonds stand for further siblings (with number of siblings indicated). Family members with PUS1 mutations are marked in black (full symbol: homozygous; half symbol: heterozygous). Gray color: not tested.