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

Black, Graeme C.; Sergouniotis, Panagiotis; Sodi, Andrea; Leroy, Bart P.; Van Cauwenbergh, Caroline; Liskova, Petra; Gronskov, Karen; Klett, Artur; Kohl, Susanne; Taurina, Gita; Sukys, Marius; Haer-Wigman, Lonneke; Nowomiejska, Katarzyna; Marques, Joao Pedro; Leroux, Dorothee; Cremers, Frans P. M.; De Baere, Elfride; Dollfus, Helene

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

Author:

Black, Graeme C.; Sergouniotis, Panagiotis; Sodi, Andrea; Leroy, Bart P.; Van Cauwenbergh, Caroline; Liskova, Petra; Gronskov, Karen; Klett, Artur; Kohl, Susanne; Taurina, Gita; Sukys, Marius; Haer-Wigman, Lonneke; Nowomiejska, Katarzyna; Marques, Joao Pedro; Leroux, Dorothee; Cremers, Frans P. M.; De Baere, Elfride; Dollfus, Helene

Tübinger Autor(en):

Kohl, Susanne

Published in:

Orphanet Journal of Rare Diseases (2021), Bd. 16, Article 142

Verlagsangabe:

Bmc

Language:

English

Full text:

http://dx.doi.org/10.1186/s13023-021-01756-x

ISSN:

1750-1172