Description

This study is looking at patients’ with Rett syndrome, MECP2 duplication, FoxG1, CNKL5 and family history related to Rett syndrome and MECP2 mutation.

The study is available to patients ages 0-65+ years old with diagnosis of Rett syndrome, MECP2 duplication, FOXG1 and CDKL5.

Contact:

Jackie Soto
Phone: (832) 822-1260
Email: jxsoto@texaschildrens.org

Contact

Jackie Soto jxsoto@texaschildrens.orgPhone 1: (832) 822-1260
IRB: h-36995

Status

Active

Created

Feb 11, 2016