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Pediatric Blood & Cancer, ISSN 1545-5009, 04/2019, Volume 66, Issue 4, pp. e27591 - n/a
Background Sideroblastic anemia represents a heterogeneous group of inherited or acquired diseases with disrupted erythroblast iron utilization, ineffective... 
MLASA | ring sideroblasts | mitochondrial disorders | mtDNA | Pearson syndrome | sideroblastic anemia | ERYTHROPOIETIN | SINGLE | MYOPATHY | PATHOPHYSIOLOGY | MUSCLE MITOCHONDRIA | GENE | ONCOLOGY | PEDIATRICS | LACTIC-ACIDOSIS | TRANSFER-RNA | MUTATIONS | SPECTRUM | HEMATOLOGY | Mitochondrial Diseases - pathology | Lipid Metabolism, Inborn Errors - genetics | Congenital Bone Marrow Failure Syndromes | Humans | Mitochondrial Diseases - metabolism | Child, Preschool | Male | Iron Overload - pathology | Anemia, Sideroblastic - metabolism | MELAS Syndrome - genetics | Iron Overload - metabolism | Lipid Metabolism, Inborn Errors - pathology | Female | Anemia, Sideroblastic - pathology | Child | Mitochondrial Diseases - genetics | Iron Overload - genetics | Lipid Metabolism, Inborn Errors - metabolism | Acyl-CoA Dehydrogenase, Long-Chain - metabolism | Muscular Diseases - metabolism | Acyl-CoA Dehydrogenase, Long-Chain - genetics | MELAS Syndrome - metabolism | Muscular Diseases - pathology | Anemia, Sideroblastic - genetics | Muscular Diseases - genetics | Acyl-CoA Dehydrogenase, Long-Chain - deficiency | Oxidases | Anemia | Refractory anemia | Cytochrome | Erythropoiesis | Cardiomyopathy | Cytochrome-c oxidase | Disorders | Iron | Sideroblastic anemia | Mitochondrial DNA | Gene deletion | Mitochondria | Children | Lactic acidosis | Phenotypes | Hematology | Sideroblasts | Patients | Renal tubular acidosis | Microencephaly | COX10 protein | Cytochromes | Sepsis | Fatalities | Mutation | Acidosis | Myopathy
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