Congenital lactose intolerance is triggered by severe mutations on both alleles of the lactase gene
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology,General Medicine
Link
http://link.springer.com/article/10.1186/s12876-015-0261-y/fulltext.html
Reference29 articles.
1. Lifshitz F. Congenital lactase deficiency. J Pediatr. 1966;69:229–37.
2. Savilahti E, Launiala K, Kuitunen P. Congenital lactase deficiency. A clinical study on 16 patients. Arch Dis Child. 1983;58:246–52.
3. Uchida N, Sakamoto O, Irie M, Abukawa D, Takeyama J, Kure S, et al. Two novel mutations in the lactase gene in a Japanese infant with congenital lactase deficiency. Tohoku J Exp Med. 2012;227:69–72.
4. Torniainen S, Freddara R, Routi T, Gijsbers C, Catassi C, Hoglund P, et al. Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD). BMC Gastroenterol. 2009;9:8.
5. Behrendt M, Keiser M, Hoch M, Naim HY. Impaired trafficking and subcellular localization of a mutant lactase associated with congenital lactase deficiency. Gastroenterology. 2009;136:2295–303.
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