Zobrazeno 1 - 2
of 2
pro vyhledávání: '"D. K. Saydaeva"'
Autor:
N. V. Petrova, N. Y. Kashirskaya, D. K. Saydaeva, A. V. Polyakov, T.A. Adyan, O. I. Simonova, Y. V. Gorinova, E. I. Kondratyeva, V. D. Sherman, O. G. Novoselova, T. A. Vasilyeva, A. V. Marakhonov, M. Macek, E. K. Ginter, R. A. Zinchenko
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-7 (2019)
Abstract Background Cystic fibrosis (CF; OMIM #219700) is a common autosomal recessive disease caused by pathogenic variants (henceforward mutations) in the cystic fibrosis transmembrane conductance regulator gene (CFTR). The spectrum and frequencies
Externí odkaz:
https://doaj.org/article/592070c75b8342d5ae78cf9010e42d83
Autor:
A. V. Polyakov, Rena A. Zinchenko, Victoria Sherman, T.A. Adyan, Nataliya Kashirskaya, O.G. Novoselova, Nika V. Petrova, Olga I. Simonova, Y. V. Gorinova, Tatyana A. Vasilyeva, Elena Kondratyeva, D. K. Saydaeva, Milan Macek, Andrey V. Marakhonov, E. K. Ginter
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-7 (2019)
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-7 (2019)
Background Cystic fibrosis (CF; OMIM #219700) is a common autosomal recessive disease caused by pathogenic variants (henceforward mutations) in the cystic fibrosis transmembrane conductance regulator gene (CFTR). The spectrum and frequencies of CFTR