TY  - GEN
AU  - Tanner,Stephan M
AU  - Li,Zhongyuan
AU  - Bisson,Ryan
AU  - Acar,Ceren
AU  - Oner,Cihan
AU  - Oner,Reyhan
AU  - Cetin,Mualla
AU  - Abdelaal,Mohamed A
AU  - Ismail,Essam A
AU  - Lissens,Willy
AU  - Krahe,Ralf
AU  - Broch,Harald
AU  - Gräsbeck,Ralph
AU  - de la Chapelle,Albert
TI  - Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East
SN  - 1098-1004
PY  - 2004///0506
KW  - Anemia, Megaloblastic
KW  - genetics
KW  - Consanguinity
KW  - DNA Mutational Analysis
KW  - Female
KW  - Founder Effect
KW  - Haplotypes
KW  - Humans
KW  - Intestinal Absorption
KW  - Male
KW  - Membrane Proteins
KW  - Middle East
KW  - Mutation
KW  - Pedigree
KW  - Proteins
KW  - Receptors, Cell Surface
KW  - Scandinavian and Nordic Countries
KW  - Vitamin B 12 Deficiency
KW  - diagnosis
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1002/humu.20014
ER  -