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Members of the mitochondrial solute carrier (SLC) family 25 (SLC25) provide transport steps for substances across the mitochondrial inner membrane into the mitochondria that are needed for biochemical pathways and cellular homoeostasis

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AcikaraB.Ion exchange chromatography and its applications

doi: 10.1016/S0022-510X(96)00197-9 62 MillerJLGrantPA

People who carry the genetic mutations that cause G6PD deficiency are at an increased risk for hemolytic anemia when taking certain medications, including quinine-based medication

Because there are no symptoms in carriers, its hard to know exactly how many people in the general population have an abnormal copy of the gene