Amir R.E. et al. 1999


Amir R.E., Van den Veyver I.., 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.

鸯铗痂蝈 蜞赕:

  • 蒿桡屙弪桕 RTT (耔礓痤 旋蝌)
  • MeCP2 耔礓痤 绣蝌 (RTT)
  • MeCP2 (体蜩-佯-疋琨忄栝 镳铗彖 2)