Rett Syndrome, MECP2 Duplication Disorder, and Rett-Related Disorders (H-36995)
Description
Content
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
Phone 1: 832–822–1260
Phone 2: 832–822–1260
IRB: H-36995
Status:
Active
Created:
