Translatability barriers between preclinical and clinical trials of AAV gene therapy in inherited retinal diseases

Shamshad, A., Kang, C., Jenny, L. A., Persad-Paisley, E. M., & Tsang, S. H. (2023). Translatability barriers between preclinical and clinical trials of AAV gene therapy in inherited retinal diseases. Vision Research, 210, 108258. https://doi.org/10.1016/j.visres.2023.108258
Authors:
Alizeh Shamshad
Chaerim Kang
Laura A Jenny
Elijah M Persad-Paisley
Stephen H Tsang
Affiliated Authors:
Laura A Jenny
Stephen H Tsang
Columbia Affiliation:
Subjects:
Dependovirus (MeSH)
Retinal Diseases (MeSH)
Author Keywords:
aav
gene therapy
inherited retinal disease
viral vector
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Publication Type:
Article
Unique ID:
10.1016/j.visres.2023.108258
PMID:
37244011
DOI:
10.1016/j.visres.2023.108258
Journal:
Vision Research
Publication Date:
Data Source:
PubMed
Source Link:
View PubMed Record
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Record Created: