Pages that link to "Q55000684"
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The following pages link to Guiding Lights in Genome Editing for Inherited Retinal Disorders: Implications for Gene and Cell Therapy. (Q55000684):
Displaying 7 items.
- Inherited Eye Diseases with Retinal Manifestations through the Eyes of Homeobox Genes (Q89944661) (← links)
- A Novel Chromosomal Translocation Identified due to Complex Genetic Instability in iPSC Generated for Choroideremia (Q90080280) (← links)
- Genome Editing as a Treatment for the Most Prevalent Causative Genes of Autosomal Dominant Retinitis Pigmentosa (Q92276489) (← links)
- Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression Profiles (Q92464626) (← links)
- Molecular Therapies for Inherited Retinal Diseases-Current Standing, Opportunities and Challenges (Q92988365) (← links)
- Ready for Repair? Gene Editing Enters the Clinic for the Treatment of Human Disease (Q98292027) (← links)
- Novel Therapeutic Approaches for the Treatment of Retinal Degenerative Diseases: Focus on CRISPR/Cas-Based Gene Editing (Q99711158) (← links)