Characterization of mecp2 function in rett syndrome

Reference:
QLK2-CT-2002-51761

Abstract:
Ret Syndrome, an important cause of mental retardation in women, is associated with mutations in the gene encoding methyl- Cog binding protein. The aim of this project is to identify target genes whose expression is altered as a result of Mapco mutations.

PROJECT DETAILS 

beginning: 2003.

end: 2005.

Country of research: Spain

Counry of funding source: EU

Funding organization: FP5-LIFE QUALITY

Financing: EU-CORDIS – 119 408 €

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