Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East. [electronic resource]
Producer: 20040506Description: 327-33 p. digitalISSN:- 1098-1004
- Anemia, Megaloblastic -- genetics
- Consanguinity
- DNA Mutational Analysis
- Female
- Founder Effect
- Haplotypes
- Humans
- Intestinal Absorption
- Male
- Membrane Proteins
- Middle East
- Mutation
- Pedigree
- Proteins -- genetics
- Receptors, Cell Surface -- genetics
- Scandinavian and Nordic Countries
- Vitamin B 12 Deficiency -- diagnosis
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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