High prevalence of W1282x mutation in cystic fibrosis patients from Karachay-Cherkessia.
暂无分享,去创建一个
B. Kerem | E. Ginter | A. Voronkova | N. Kashirskaya | V. Sherman | N. Kapranov | R. Zinchenko | E. Kondratyeva | N. Petrova | T. Vasilyeva | A. Makaov | O. Novoselova | E. E. Timkovskaya | L. Shabalova
[1] G. Lukács,et al. Some gating potentiators, including VX-770, diminish ΔF508-CFTR functional expression , 2014, Science Translational Medicine.
[2] A. Polyakov,et al. Mutation p.E92K is the primary cause of cystic fibrosis in Chuvashes , 2012, Russian Journal of Genetics.
[3] L. Excoffier,et al. Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows , 2010, Molecular ecology resources.
[4] R. Guseynov. Judaism in the Caucasus , 2008 .
[5] B. Kerem,et al. Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis , 1993, Human Genetics.
[6] E. Ginter,et al. [Portion of certain cystic fibrosis gene mutations and linkage dysequilibrium between the CFTR-gene locus and two DNA marker loci in Russian populations]. , 1994, Genetika.