DOI:
10.1055/s-00000041
Neuropediatrics
LinksClose Window
References
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;
23 (2) 185-188
Search in:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.