Rett syndrome is caused by mutations of the MECP2 gene located on the X chromosome ... breathing difficulties and seizures ...
The MECP2 mutations were divided into four different ... year before examination date and could be obtained. An experienced child radiologist evaluated the radiographs according to Genant's ...
Alteration in the expression of methyl-CpG-binding protein 2 (MeCP2) has been linked to a number of neurological disorders, including Rett syndrome (RTT). A recent modifier screen in flies has ...