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pro vyhledávání: '"Vichithra R.B. Liyanage"'
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 8, p 1845 (2019)
Methyl CpG binding protein-2 (MeCP2) isoforms (E1 and E2) are important epigenetic regulators in brain cells. Accordingly, MeCP2 loss- or gain-of-function mutation causes neurodevelopmental disorders, including Rett syndrome (RTT), MECP2 duplication
Externí odkaz:
https://doaj.org/article/d7f136ad28c64ac9b4d1fd967bf2d291