This database has been constructed by merging mutation and polymorphism data from the published literature pertaining to Rett syndrome and related clinical disorders, and by incorporating unpublished mutation and polymorphism data that have been submitted directly to us. Information can only be submitted by clinicians or the testing labs. Please encourage your child's doctor to contribute to this database by completing the MECP2 Mutation Data Form.
RettBASE is curated by: Prof. John Christodoulou. The MECP2 database and website are maintained by the Western Sydney Genetics Program.
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