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doi: 10.1146/annurev.publhealth.28.021406.144007

10.1038/s41556-018-0178-0 129 ZhangY.TanH.DanielsJ

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The discovery of a sideroblastic anemia patient with a GLRX5 mutation suggests that components of the FeS cluster assembly machinery should be assessed in the abnormal erythroid cells from patients with sideroblastic anemias of unknown cause, because mutations of genes in the FeS pathway could arise in bone marrow stem cells in mature individuals whose germline cells would be unaffected

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doi: 10.1515/acph-2017-0023 233 De WaureCBertolaCBaccariniGChiavariniMMancusoC