Rett Syndrome, MECP2 Duplication Disorder, and Rett-Related Disorders (H-36995)
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.
Phone: (832) 822-1260
Phone 1: 832–822–1260
Phone 2: 832–822–1260