Different pathophysiological mechanisms of intramitochondrial iron accumulation in acquired and congenital sideroblastic anemia caused by mitochondrial DNA deletion. [electronic resource]
Producer: 20060913Description: 169-74 p. digitalISSN:- 0902-4441
- Acidosis -- genetics
- Adolescent
- Anemia, Refractory -- genetics
- Anemia, Sideroblastic -- genetics
- Bone Marrow -- pathology
- Cytochrome-c Oxidase Deficiency -- genetics
- DNA Mutational Analysis
- DNA, Mitochondrial -- genetics
- Disease Progression
- Electron Transport
- Electron Transport Complex IV -- analysis
- Fatal Outcome
- Gene Deletion
- Heterozygote
- Humans
- Iron -- metabolism
- Male
- Mitochondria -- metabolism
- Mitochondrial Myopathies -- blood
- Mitochondrial Proton-Translocating ATPases -- deficiency
- Mosaicism
- RNA, Transfer -- genetics
- beta-Thalassemia -- genetics
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Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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