Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet. 1999 Oct;23(2):185-8. PubMed.

Recommends

Please login to recommend the paper.

Comments

No Available Comments

Make a Comment

To make a comment you must login or register.

This paper appears in the following:

News

  1. Multitasking Rett Protein Shines Spotlight on RNA Splicing in Neurologic and Psychiatric Disease
  2. Research Brief: MECP2 Gene Variants Take a Piece of Your Mind
  3. Novel Methylation Distinguishes Neuron Types, May Dictate Disease