Citations for
1LCT
Mutations in the Translated Region of the Lactase Gene (LCT) Underlie Congenital Lactase Deficiency.
Kuokkanen M, Kokkonen J, Enattah NS, Ylisaukko-Oja T, Komu H, Varilo T, Peltonen L, Savilahti E, Jarvela I.
Am J Hum Genet 78(2):339-44. Epub 2005 Dec 15. 2006
2LCT
Identification of a variant associated with adult-type hypolactasia.
Enattah NS, Sahi T, Savilahti E, Terwilliger JD, Peltonen L, Jarvela I.
Nat Genet 30(2):233-7. 2002
3LCT
Common polymorphism in a highly variable region upstream of the human lactase gene affects DNA-protein interactions.
Hollox EJ, et al.
Eur J Hum Genet 7(7):791-800 1999
4LCT, LDC
Assignment of the locus for congenital lactase deficiency to 2q21, in the vicinity of but separate from the lactase-phlorizin hydrolase gene.
JŠrvelŠ I, et al.
Am J Hum Genet 63 : 1078-1085. 1998
5LCT, MCM6
Characterisation of a human homologue of a yeast cell division cycle gene, MCM6, located adjacent to the 5' end of the lactase gene on chromosome 2q21.
Harvey CB, et al.
FEBS Lett 398 : 135-140. 1996
6LCT
The lactase persistence/non-persistence polymorphism is controlled by a cis-acting element.
Wang Y, et al.
Hum Mol Genet 4 : 657-662. 1995
7LCT
DNA polymorphisms in the lactase gene. Linkage disequilibrium across the 70-kb region.
Harvey CB, et al.
Eur J Hum Genet 3 : 27-41. 1995
8LCT
Regional localization of the lactase-phlorizin hydrolase gene, LCT, to chromosome 2q21.
Harvey CB, et al.
Ann Hum Genet 57 : 179-185. 1993
9LCT
Regulation of intestinal lactase in adult hypolactasia.
Lloyd M, et al.
J Clin Invest 89 : 524-529. 1992
10LCT, LDC
Structure of the chromosomal gene and cDNAs coding for lactase-phlorizin hydrolase in humans with adult-type hypolactasia or persistence of lactase.
Boll W, et al.
Am J Hum Genet 48 : 889-902. 1991
11LCT, LDC
Molecular analysis of the lactase gene in the congenital lactase deficiency.
Poggi V, et al.
Am J Hum Genet 49S : 105. 1991
12LCT
The human lactase-phlorizin hydrolase gene is located on chromosome 2.
Kruse TA, Bolund L, Grzeschik KH, Ropers HH, Sjostrom H, Noren O, Mantei N, Semenza G.
FEBS Lett 240 : 123-126. 1988