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: 7NR1/1 Abstract: PROJECT DETAILS beginning: n.a end: n.a Country of research: Italy, US Counry of funding source: United States Funding organization: Bilateral Italy (ISS)ﾗUSA (NIH, Office for rare diseases) Financing: NATIONAL FUNDINGS – 0 € hyperlink
Reference: ANR-12n.a.003-BSV1 Abstract: The MeCP2-pathies represent a field of particularly dynamic and competitive research in the field of intellectual disabilities related to the X chromosomeﾠRett syndrome (RTT) is the prototype of these diseases and account for 10% of cases of mental retardation of genetic origin in women.ﾠThe causative gene is Mecp2 encoding a multifunctional protein … Read more
Reference: ANR-12n.a.003-BSV1 Abstract: The MeCP2-pathies represent a field of particularly dynamic and competitive research in the field of intellectual disabilities related to the X chromosome Rett syndrome (RTT) is the prototype of these diseases and account for 10% of cases of mental retardation of genetic origin in women. The causative gene is Mecp2 encoding a … Read more
Reference: P09-CTS-4610 Abstract: n.a PROJECT DETAILS beginning: 2010. end: 2014. Country of research: Spain Counry of funding source: Spain Funding organization: Junta de Andaluc�a (Regional Ministry of Innovation, Science and Business) Financing: NATIONAL FUNDINGS – 178 671 € hyperlink
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