Wanes, D., Husein, D. M., & Naim, H. Y. (2019). Congenital Lactase Deficiency: Mutations, Functional and Biochemical Implications, and Future Perspectives. Nutrients, 11(2), 461. https://doi.org/10.3390/nu11020461
Torniainen, S., Freddara, R., Routi, T., Gijsbers, C., Catassi, C., Höglund, P., Savilahti, E., & Järvelä, I. (2009). Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD). BMC gastroenterology, 9, 8. https://doi.org/10.1186/1471-230X-9-8
Fazeli, W., Kaczmarek, S., Kirschstein, M. ym. A novel mutation within the lactase gene (LCT): the first report of congenital lactase deficiency diagnosed in Central Europe. BMC Gastroenterol 15, 90 (2015). https://doi.org/10.1186/s12876-015-0316-0
Uchida N, Sakamoto O, Irie M, Abukawa D, Takeyama J, Kure S, Tsuchiya S. Two novel mutations in the lactase gene in a Japanese infant with congenital lactase deficiency. Tohoku J Exp Med. 2012 May;227(1):69-72. https://doi.org/10.1620/tjem.227.69
duodecimlehti.fi
Torniainen, S., Savilahti, E., & Järvelä, I. (2009). Synnynnäinen laktaasinpuute-arvioitua yleisempi sairaus?:[katsaus]. Duodecim, 125(7), 766-770. https://www.duodecimlehti.fi/duo97968
huslab.fi
HUSLAB (2020) Synnynnäinen laktaasinpuutos, laktaasigeenin valtamutaation tutkimus verestä, Helsingin yliopistollinen sairaala [luettu 10.11.2020] https://huslab.fi/ohjekirja/20118.html