Amir R.E. et al. 1999


Amir R.E., Van den Veyver I.Â., Wan M., Tran C.Q., Francke U., and Zoghbi H.Y., 1999. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat. Genet. 23: 185-188.

Ñìîòðèòå òàêæå:

  • Ýïèãåíåòèêà è RTT (ñèíäðîì Ðýòòà)
  • MeCP2 è ñèíäðîì Ðåòòà (RTT)
  • MeCP2 (Ìåòèë-ÑðÑ-ñâÿçûâàþùèé ïðîòåèí 2)