Adult type hypolactasia in an ethnic Uzbek population.
Correlation of G/A-22018 single-nucleotide polymorphism with lactase activity and its usefulness in improving the diagnosis of adult-type hypolactasia among North Indian children.
Introducing genetic testing for adult-type hypolactasia.
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.
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.
T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of adult-type hypolactasia in an Arab population(s).
The C/C(-13910) and G/G(22018) genotypes for adult-type hypolactasia are not associated with inflammatory bowel disease.
Transcriptional regulation of the lactase-phlorizin hydrolase gene by polymorphisms associated with adult-type hypolactasia.
Single-nucleotide polymorphisms upstream from the lactase gene have been associated with adult-type hypolactasia (33, 34) and tested to identify individuals with genetic disposition for this disorder (35, 36).
The method optimized in this work is, therefore, ready for clinical trials, so that it might be applied within the primary healthcare system as a convenient, noninvasive new test for diagnosis of hypolactasia.
13910] genotype concur with the prevalence of primary adult hypolactasia (2).
Tests for the diagnosis of hypolactasia consist of biochemical tests such as the lactose breath hydrogen test (LBHT), lactase enzyme activity tests performed with biopsy samples of the small intestine, and most recently, molecular tests to determine the allelic variants of LPH C [right arrow] [T.