Biogenic amines and their metabolites are differentially affected in the <it>Mecp2</it>-deficient mouse brain
<p>Abstract</p> <p>Background</p> <p>Rett syndrome (RTT, MIM #312750) is a severe neurological disorder caused by mutations in the X-linked methyl-CpG binding protein 2 (<it>MECP2</it>) gene. Female patients are affected with an incidence of 1/15000 live bir...
| Main Authors: | , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
BMC
2011-05-01
|
| Series: | BMC Neuroscience |
| Online Access: | http://www.biomedcentral.com/1471-2202/12/47 |