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Biochemical and genetic defects underlying human congenital hypotransferrinemia
Biochemical and genetic defects underlying human congenital hypotransferrinemia
- Publication Year :
- 2000
-
Abstract
- Human congenital hypotransferrinemia is a rare disorder characterized by the virtual absence of transferrin in the serum. No information on the causes of the disease is known.
Details
- Database :
- OAIster
- Notes :
- English
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.on1308912580
- Document Type :
- Electronic Resource