Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns. [electronic resource]
Producer: 20130214Description: 56 p. digitalISSN:- 1750-1172
- Anemia, Megaloblastic
- Ethnicity -- genetics
- Female
- Founder Effect
- Genetic Association Studies
- Genetic Heterogeneity
- Genetic Testing
- Humans
- Intrinsic Factor -- genetics
- Malabsorption Syndromes -- ethnology
- Male
- Membrane Proteins
- Mutation
- Proteins -- genetics
- Proteinuria -- ethnology
- Vitamin B 12 -- metabolism
- Vitamin B 12 Deficiency -- ethnology
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Publication Type: Journal Article; Research Support, N.I.H., Extramural
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