Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East.

Tanner, Stephan M

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] - Human mutation Apr 2004 - 327-33 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

1098-1004

10.1002/humu.20014 doi


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