Natural history of recessive inheritance of DMT1 mutations. [electronic resource]
Producer: 20080107Description: 136-9 p. digitalISSN:- 1097-6833
- Anemia, Hypochromic -- diagnosis
- Cation Transport Proteins -- deficiency
- Diagnosis, Differential
- Erythrocytes -- metabolism
- Erythropoietin -- therapeutic use
- Ferritins -- blood
- Genes, Recessive
- Genotype
- Humans
- Infant, Newborn
- Iron Chelating Agents -- therapeutic use
- Mutation
- Phenotype
- Transferrin -- metabolism
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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