A new role for MeCP2 in the repair of DNA.

Reference: Dr. Giglia-Mari Abstract: n.a PROJECT DETAILS  beginning: 2012. end: 2014. Country of research: France Counry of funding source: France Funding organization: French Association Rett Syndrome Financing: PRIVATE FUNDERS – 30 000 € hyperlink

Molecular pathologies and functional interactions of the X-linked MECP2 and CDKL5 genes

Reference: Charlotte Kilstrup-Nielsen Abstract: Rett syndrome (RTT) is a severe pediatric neurological disorder that, because of its incidence, represents the most common genetic cause of severe intellectual disability in girls worldwide. Several RTT variants have been described ranging from milder forms with a later age of onset to conditions with very early severe epileptic manifestations. … Read more

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