Prevalence of adult-type hypolactasia as diagnosed with genetic and lactose hydrogen breath tests in Hungarians-Reference-Cited by-同舟云学术

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Prevalence of adult-type hypolactasia as diagnosed with genetic and lactose hydrogen breath tests in Hungarians

Published:2009-01-21 Issue:7 Volume:63 Page:909-912
ISSN:0954-3007
Container-title:European Journal of Clinical Nutrition
language:en
Short-container-title:Eur J Clin Nutr

Author:

Nagy D,Bogácsi-Szabó E,Várkonyi Á,Csányi B,Czibula Á,Bede O,Tari B,Raskó I

Publisher

Springer Science and Business Media LLC

Subject

Nutrition and Dietetics,Medicine (miscellaneous)

Link

http://www.nature.com/articles/ejcn200874.pdf

Reference20 articles.

1. Arola H, Koivula T, Jokela H, Jauhiainen M, Keyrilainen O, Hola T et al. (1988). Comparison of indirect diagnostic methods for hypolactasia. Scand J Gastroenterol Suppl 23, 351–357.

2. Bernardes-Silva CF, Pereira AC, Fátima Alves da Mota G, Krieger JE, Laudanna AA (2007). Lactase persistence/non-persistence variants, C/T_13910 and G/A_22018, as a diagnostic tool for lactose intolerance in IBS patients. Clin Chim Acta 386, 7–11.

3. Büning C, Genschel J, Jurga J, Fiedler T, Voderholzer W, Fiedler EM et al. (2005). Introducing genetic testing for adult-type hypolactasia. Digestion 71, 245–250.

4. Enattah NS, Jensen TG, Nielsen M, Lewinski R, Kuokkanen M, Rasinperä H et al. (2008). Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk culture. Am J Hum Genet 82, 57–72.

5. Enattah NS, Sahi T, Savilahti E, Terwilliger JD, Peltonen L, Järvelä I (2002). Identification of a variant associated with adult-type hypolactasia. Nat Genet 30, 233–237.

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