Meins M. et al. 2005


Meins M., Lehmann J., Gerresheim F., Herchenbach J., Hagedorn M., Hameister K., and Epplen J.T., 2005. Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome. J. Med. Genet. 42: el2.

Смотрите также:

  • Эпигенетика и RTT (синдром Рэтта)