Downstream Effects of MECP1 Mutations in Rett Syndrome and other forms of X-linked mental retardation Studied by cDNA arrays (C 3)

Reference:
C3 – Subproject to SFB 577: Molecular Basis of Clinical variability in Mendelian Disorders

Abstract:

PROJECT DETAILS 

beginning: 2001.

end: 2004.

Country of research: Germany

Counry of funding source: Germany

Funding organization: GermanﾠResearch Foundation

Financing: NATIONAL FUNDINGS – 0 €

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