ISSN:
1546-1718
Source:
Nature Archives 1869 - 2009
Topics:
Biology
,
Medicine
Notes:
[Auszug] Rett syndrome (RTT) is a severe neurodevelopmental disorder that affects girls almost exclusively. Approximately 80% of classical RTT cases are caused by mutations in MECP2, a transcriptional silencer that can bind any DNA sequence containing at least a CpG island. On the basis of this function, it ...
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1038/ng0105-10