The purpose of this study is to advance understanding of the natural history of Rett syndrome (RTT), MECP2-duplication disorder (MECP2 Dup), RTT-related disorders including CDKL5, FOXG1, and individuals with MECP2 mutations who do not have RTT. Samples with DNA will be collected. Click here to view the study.
University of Alabama, Birmingham
For more information, please contact Jane Lane at [email protected] or Dr. Alan Percy.