The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement.
- DOI
- 10.1186/s13023-021-01756-x
- Published
- 2021 Mar 20
- Container
- Orphanet journal of rare diseases
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-021-01756-x,
title = {The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement.},
author = {Black GC and Sergouniotis P and Sodi A and Leroy BP and Van Cauwenbergh C and Liskova P and Grønskov K and Klett A and Kohl S and Taurina G and Sukys M and Haer-Wigman L and Nowomiejska K and Marques JP and Leroux D and Cremers FPM and De Baere E and Dollfus H and ERN-EYE study group},
year = {2021},
journal = {Orphanet journal of rare diseases},
doi = {10.1186/s13023-021-01756-x},
url = {https://doi.org/10.1186/s13023-021-01756-x}
}RIS
TY - JOUR TI - The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement. AU - Black GC AU - Sergouniotis P AU - Sodi A AU - Leroy BP AU - Van Cauwenbergh C AU - Liskova P AU - Grønskov K AU - Klett A AU - Kohl S AU - Taurina G AU - Sukys M AU - Haer-Wigman L AU - Nowomiejska K AU - Marques JP AU - Leroux D AU - Cremers FPM AU - De Baere E AU - Dollfus H AU - ERN-EYE study group PY - 2021 JO - Orphanet journal of rare diseases DO - 10.1186/s13023-021-01756-x UR - https://doi.org/10.1186/s13023-021-01756-x ER -
APA
GC, B., P, S., A, S., BP, L., C, V. C., P, L., K, G., A, K., S, K., G, T., M, S., L, H., K, N., JP, M., D, L., FPM, C., E, D. B., H, D., & group, E. S. (2021). The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-021-01756-x
Source records
- pubmed · retrieved 2026-09-26T13:54:54.766Z
- europe-pmc · retrieved 2026-09-26T13:54:54.764Z
- doaj · retrieved 2026-09-26T13:54:54.741Z
- hal · retrieved 2026-09-26T13:54:54.988Z