Zobrazeno 1 - 1
of 1
pro vyhledávání: '"E. M. Shitik"'
Autor:
I. V. Grishchenko, A. A. Tulupov, Y. M. Rymareva, E. D. Petrovskiy, A. A. Savelov, A. M. Korostyshevskaya, Y. V. Maksimova, A. R. Shorina, E. M. Shitik, D. V. Yudkin
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 25, Iss 1, Pp 117-124 (2021)
There are more than 30 inherited human disorders connected with repeat expansion (myotonic dystrophy type I, Huntington’s disease, Fragile X syndrome). Fragile X syndrome is the most common reason for inherited intellectual disability in the human
Externí odkaz:
https://doaj.org/article/835788c2a5e54b3d8c2c1d7e057dffd0
