A Phenotypic Study of CRB1 Retinopathy Secondary to the Variant p.(Pro836Thr) Prevalent in Those of Black African Ancestry.
- DOI
- 10.1167/iovs.66.9.3
- Published
- 2025 Jul 1
- Container
- Investigative ophthalmology & visual science
- Publisher
- Not recorded
- Open access
- yes
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limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.1167/iovs.66.9.3,
title = {A Phenotypic Study of CRB1 Retinopathy Secondary to the Variant p.(Pro836Thr) Prevalent in Those of Black African Ancestry.},
author = {Wong WM and Robson AG and Baker RA and Arno G and Van Aerschot J and Lin S and Moosajee M and Michaelides M and Mahroo OA and Webster AR},
year = {2025},
journal = {Investigative ophthalmology \& visual science},
doi = {10.1167/iovs.66.9.3},
url = {https://doi.org/10.1167/iovs.66.9.3}
}RIS
TY - JOUR TI - A Phenotypic Study of CRB1 Retinopathy Secondary to the Variant p.(Pro836Thr) Prevalent in Those of Black African Ancestry. AU - Wong WM AU - Robson AG AU - Baker RA AU - Arno G AU - Van Aerschot J AU - Lin S AU - Moosajee M AU - Michaelides M AU - Mahroo OA AU - Webster AR PY - 2025 JO - Investigative ophthalmology & visual science DO - 10.1167/iovs.66.9.3 UR - https://doi.org/10.1167/iovs.66.9.3 ER -
APA
WM, W., AG, R., RA, B., G, A., J, V. A., S, L., M, M., M, M., OA, M., & AR, W. (2025). A Phenotypic Study of CRB1 Retinopathy Secondary to the Variant p.(Pro836Thr) Prevalent in Those of Black African Ancestry.. Investigative ophthalmology & visual science. https://doi.org/10.1167/iovs.66.9.3
Source records
- pubmed · retrieved 2026-09-26T01:00:14.221Z
- europe-pmc · retrieved 2026-09-26T01:00:14.238Z