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Split-Intein Mediated Full-Length SMCHD1 Gene Replacement Therapy for FSHD
TS-004612 — This IP is a therapeutic strategy for facioscapulohumeral dystrophy (FSHD), which is associated with an inappropriate expression of DUX4. Using dual AAV split-intein vectors, it expresses full-length SMCHD1, enhances epigenetic silencing and reduces DUX4 toxicity.
  • College:
  • Inventors: Harper, Scott; Thangaraj, Merlin Premalatha
  • Licensing Officer: Eidahl, Jocelyn

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