Biobanking of Rett Syndrome and Related Disorders

Biobanking of Rett Syndrome and Related Disorders


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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. This study will be conducted at Boston
Children’s Hospital.¬† It is led by Mustafa Sahin, MD, PhD.

For more information, email [email protected].