Reference: B11 – Subproject to SFB 665: Developmental disorders in the nervous system Abstract: PROJECT DETAILS beginning: 2009. end: n.a Country of research: Germany Counry of funding source: Germany Funding organization: GermanﾠResearch Foundation Financing: NATIONAL FUNDINGS – 0 € hyperlink
Reference: ORPHA 94817 Abstract: PROJECT DETAILS beginning: n.a end: n.a Country of research: France Counry of funding source: France Funding organization: Ministry of Social Issues Financing: NATIONAL FUNDINGS – 0 € hyperlink
Reference: ORPHA 231931 Abstract: PROJECT DETAILS beginning: n.a end: n.a Country of research: Germany Counry of funding source: Germany Funding organization: German Research Foundation Financing: NATIONAL FUNDINGS – 0 € hyperlink
Reference: ORPHA267379 Abstract: PROJECT DETAILS beginning: n.a end: n.a Country of research: Germany Counry of funding source: Germany Funding organization: German Research Foundation Financing: NATIONAL FUNDINGS – 0 € hyperlink
Reference: Abstract: Mecp2-pathies represent an emerging field among severe X-linked mental retardation syndromes. Rett Syndrome (RTT) represents the prototype of these pathologies and accounts for 10% of the cases of profound intellectual disability in females. The causative gene is the methyl CpG-binding protein 2 (MECP2) gene, encoding a multifunctional protein thought to ﾫmodulateﾫ the expression … Read more
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