Author:
Borinskaya S. A.,Rebrikov D. V.,Nefedova V. V.,Kofiadi I. A.,Sokolova M. V.,Kolchina E. V.,Kulikova E. A.,Chernyshov V. N.,Kutsev S. I.,Polonikov A. V.,Ivanov V. P.,Kozlov A. I.,Yankovsky N. K.
Subject
Structural Biology,Biophysics
Reference25 articles.
1. Kuokkanen M., Kokkonen J., Enattah N.S., Ylisaukko-Oja T., Komu H., Varilo T., Peltonen L., Savilahti E., Jarvela I. 2006. Mutations in the translated region of the lactase gene (LCT) underlie congenital lactase deficiency. Am. J. Hum. Genet. 78, 339–344.
2. Kozlov A.I. 1996. Gipolaktaziya: rasprostranennost’, diagnostika, vrachebnaya taktika (Hypolactasia: Prevalence, Diagnosis, and Therapeutic Tactics). Moscow: ArktAn-S.
3. Kozlov A., Lisitsyn D. 1996. “The milk habit” (hypolactasia) in Finno-Ugrian peoples: A crossroad of physical anthropology, ethnology, and linguistics. Finnisch-Ugrische Mitteilungen. 18/19, 67–81.
4. Kozlov A.I., Balanovskaya E.V., Nurbaev S.D., Balanovskii O.P. 1998. Gene geography of primary hypolactasia in the Old World populations. Genetika. 34, 551–561.
5. Nose O., Iida Y., Kai H., Harada T., Ogawa M., Yabuuchi H. 1979. Breath hydrogen test for detecting lactose malabsorption in infants and children. Prevalence of lactose malabsorption in Japanese children and adults. Arch. Dis. Child. 54, 436–440.
Cited by
10 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献