Gene-based treatment options for Usher type 1C by translational read-through of a nonsense mutation

Παρόμοια τεκμήρια

• A comparative evaluation of NB30, NB54 and PTC124 in translational read-through efficacy for treatment of an USH1C nonsense mutation
  ανά: Goldmann, Tobias, κ.ά.
  Έκδοση: (2012)
• Translational Read-Through Therapy of RPGR Nonsense Mutations
  ανά: Vössing, Christine, κ.ά.
  Έκδοση: (2020)
• Ataluren for the Treatment of Usher Syndrome 2A Caused by Nonsense Mutations
  ανά: Samanta, Ananya, κ.ά.
  Έκδοση: (2019)
• Translational Read-Through of a Nonsense Mutation Causing Bartter Syndrome
  ανά: Cho, Hee Yeon, κ.ά.
  Έκδοση: (2013)
• Translational read-through of a nonsense mutation in ATP7A impacts treatment outcome in Menkes disease
  ανά: Kaler, Stephen G., κ.ά.
  Έκδοση: (2009)