RPE65-associated inherited retinal diseases: consensus recommendations for eligibility to gene therapy.
- DOI
- 10.1186/s13023-021-01868-4
- Published
- 2021 Jun 4
- Container
- Orphanet journal of rare diseases
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-021-01868-4,
title = {RPE65-associated inherited retinal diseases: consensus recommendations for eligibility to gene therapy.},
author = {Sodi A and Banfi S and Testa F and Della Corte M and Passerini I and Pelo E and Rossi S and Simonelli F and Italian IRD Working Group},
year = {2021},
journal = {Orphanet journal of rare diseases},
doi = {10.1186/s13023-021-01868-4},
url = {https://doi.org/10.1186/s13023-021-01868-4}
}RIS
TY - JOUR TI - RPE65-associated inherited retinal diseases: consensus recommendations for eligibility to gene therapy. AU - Sodi A AU - Banfi S AU - Testa F AU - Della Corte M AU - Passerini I AU - Pelo E AU - Rossi S AU - Simonelli F AU - Italian IRD Working Group PY - 2021 JO - Orphanet journal of rare diseases DO - 10.1186/s13023-021-01868-4 UR - https://doi.org/10.1186/s13023-021-01868-4 ER -
APA
A, S., S, B., F, T., M, D. C., I, P., E, P., S, R., F, S., & Group, I. I. W. (2021). RPE65-associated inherited retinal diseases: consensus recommendations for eligibility to gene therapy.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-021-01868-4
Source records
- pubmed · retrieved 2026-09-25T22:19:45.605Z