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478 : Mutation-specific siRNA Knockdown of GJB2 − Potential gene therapy for Keratitis-ichthyosis-deafness Syndrome

Researchers

Presenter

  • M. Lee

Principal Investigators

  • V.A. Kinsler

  • S.L. Hart

  • W. Di

Medical Centers

  • UCL GOS ICH, London, England, United Kingdom

Locations

  • United Kingdom

Companies

  • N/A

Study Components

Therapeutic Area

  • Genetic Disorder

Disease

  • Keratitis ichthyosis deafness

  • Bart-Pumphrey syndrome

Biomarkers

  • N/A

Drug/Treatment

  • N/A

Outcome

  • N/A

Study Design

  • N/A

Phase

  • NA

Study Id's

  • N/A

Sponsors

  • N/A

Result

  • Final

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