Frequency of LCT-13910C/T and LCT-22018G/A single nucleotide polymorphisms associated with adult-type hypolactasia/lactase persistence among Israelis of different ethnic groups-Reference-Cited by-同舟云学术

Frequency of LCT-13910C/T and LCT-22018G/A single nucleotide polymorphisms associated with adult-type hypolactasia/lactase persistence among Israelis of different ethnic groups

Published:2013-04 Issue:1 Volume:519 Page:67-70
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Raz Maytal,Sharon Yael,Yerushalmi Baruch,Birk Ruth

Funder

Israeli Ministry of Health

Dairy Council Research Foundation

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference28 articles.

1. Prevalence and trends in adult-type hypolactasia in different age cohorts in Central Sweden diagnosed by genotyping for the adult-type hypolactasia-linked LCT-13910C>T mutation;Almon;Scand J Gastroenterol,2007

2. Frequency of lactose malabsorption among healthy southern and northern Indian populations by genetic analysis and lactose hydrogen breath and tolerance tests;Babu;Am. J. Clin. Nutr.,2010

3. Genotyping of the lactase-phlorizin hydrolase -13910 polymorphism by LightCycler PCR and implications for the diagnosis of lactose intolerance;Bodlaj;Clin. Chem.,2006

4. Correlation between lactose absorption and the C/T-13910 and G/A-22018 mutations of the lactase-phlorizin hydrolase (LCT) gene in adult-type hypolactasia;Bulhões;Braz. J. Med. Biol. Res.,2007

5. Identification of a variant associated with adult-type hypolactasia;Enattah;Nat. Genet.,2002

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