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; Li, Zhongyuan; Bisson, Ryan; Acar, Ceren; Oner, Cihan; Oner, Reyhan; Cetin, Mualla; Abdelaal, Mohamed A; Ismail, Essam A; Lissens, Willy; Krahe, Ralf; Broch, Harald; Gräsbeck, Ralph; de la Chapelle, Albert

Tanner, Stephan M; Li, Zhongyuan; Bisson, Ryan; Acar, Ceren; Oner, Cihan; Oner, Reyhan; Cetin, Mualla; Abdelaal, Mohamed A; Ismail, Essam A; Lissens, Willy; Krahe, Ralf; Broch, Harald; Gräsbeck, Ralph; de la Chapelle, Albert.

Affiliation

Tanner SM; Human Cancer Genetics Program, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio 43210, USA.

Hum Mutat ; 23(4): 327-33, 2004 Apr.

Article in En | MEDLINE | ID: mdl-15024727

Subject(s)

Anemia, Megaloblastic/genetics; Founder Effect; Mutation; Vitamin B 12 Deficiency/genetics; Consanguinity; DNA Mutational Analysis; Female; Haplotypes; Humans; Intestinal Absorption; Male; Membrane Proteins; Middle East; Pedigree; Proteins/genetics; Receptors, Cell Surface/genetics; Scandinavian and Nordic Countries; Vitamin B 12 Deficiency/diagnosis

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Collection: 01-internacional Database: MEDLINE Main subject: Vitamin B 12 Deficiency / Founder Effect / Anemia, Megaloblastic / Mutation Type of study: Diagnostic_studies Limits: Female / Humans / Male Country/Region as subject: Asia / Europa Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2004 Document type: Article Affiliation country: United States Country of publication: United States

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