MECP2 y MeCP2

 

 

 

 

 

 

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY.

Nat Genet. 1999 Oct;23(2):185-8.

PMID: 10508514

 

Rett Syndrome and MeCP2

Liyanage VR, Rastegar M.

Neuromolecular Med. 2014 Mar 11. [Epub ahead of print]

PMID: 24615633

 

MeCP2: the long trip from a chromatin protein to neurological disorders

Ausió J, Paz AM, Esteller M.

Trends Mol Med. 2014 Apr 21. pii: S1471-4914(14)00056-2. doi: 10.1016/j.molmed.2014.03.004. [Epub ahead of print] Review.

PMID: 24766768