The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement.

Black GC, Sergouniotis P, Sodi A, Leroy BP, Van Cauwenbergh C, Liskova P, Grønskov K, Klett A, Kohl S, Taurina G, Sukys M, Haer-Wigman L, Nowomiejska K, Marques JP, Leroux D, Cremers FPM, De Baere E, Dollfus H, ERN-EYE study group

Open source

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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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

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