Extending genotype-phenotype studies of Rett syndrome using the British Isles Rett Survey database and the Rett Syndrome Behaviour Question

Reference: Dr MarkᅠBailey Abstract: n.a PROJECT DETAILS  beginning: 2004. end: 2005. Country of research: United Kingdom Counry of funding source: United Kingdom Funding organization: Rett Syndrome Association Scotland Financing: PRIVATE FUNDERS – 0 € hyperlink

Identification and characterization of proteins that, interacting with mecp2, could be involved in Rett syndrome

Reference: GP0072Y01 Abstract: Rett syndrome (RTT) is a genetic disease that occurs almost exclusively in females, with an estimated prevalence of 1 in 10.000-15.000 female births. After normal development up to the age of 6-18 months, follows a period of regression of motor and mental abilities. Affected patients develop loss of speech and purposeful hand … Read more

By continuing to use the site, you agree to the use of cookies. more information

The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.

Close