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.
