Molecular Analysis of Rett Syndrome: Mutation and Functional Analysis of MECP2 and Related Genes in Pathogenesis of Rett Syndrome

  • Barrett, Timothy (Principal Investigator)
  • Latif, Farida (Co-Investigator)
  • Turner, Bryan (Co-Investigator)
  • Webb, Teresa (Co-Investigator)

Project Details

Short titleMolecular Analysis of Rett Syndrome: Mutation and Functional Analysis of MECP2 and Related Genes in Pathogenesis of Rett Syndrome
StatusFinished
Effective start/end date1/10/0031/05/03

Funding

  • UHB CHARITABLE FUNDS