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Content archived on 2024-05-27

Characterization of mecp2 function in rett syndrome

Objective

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.

Fields of science (EuroSciVoc)

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Call for proposal

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Coordinator

CENTRO NACIONAL DE INVESTIGATIONES ONCOLOGICAS
EU contribution
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Address
C/ Melchor Fernandes Almagro, 3
28029 MADRID
Spain

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Total cost
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