Copper deficiency myelopathy and subacute combined degeneration of the cord - why is the phenotype so similar? [electronic resource]
Producer: 20080919Description: 229-36 p. digitalISSN:- 0306-9877
- 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase -- metabolism
- Copper -- deficiency
- Electron Transport Complex IV -- metabolism
- Humans
- Methylation
- Methylmalonyl-CoA Mutase -- metabolism
- Models, Biological
- Models, Theoretical
- Nitrous Oxide -- metabolism
- Phenotype
- Spinal Cord Diseases -- diagnosis
- Subacute Combined Degeneration -- diagnosis
- Vitamin B 12 Deficiency -- complications
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Publication Type: Journal Article
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