Downstream Effects of MECP1 Mutations in Rett Syndrome and other Forms of X-linked Mental Retardation studied by cDNA Arrays (C 3)

• Subject Area: Human Genetics
• Term: from 2001 to 2004
• Project identifier: Deutsche Forschungsgemeinschaft (DFG) - Project number 5484647

No abstract available

• DFG Programme: Collaborative Research Centres
• Subproject of: SFB 577: Molecular Basis of Clinical Variability in Mendelian Disorders
• Applicant Institution: Humboldt-Universität zu Berlin
• Co-Applicant Institution: Max-Planck-Institut für molekulare Genetik (MPIMG)
• Project Heads: Professorin Dr. Ulrike Nuber; Professor Dr. Hans Hilger Ropers