Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease

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Dades bibliogràfiques
Publicat a:Genet Med
Autors principals: Van de Sompele, Stijn, Smith, Claire, Karali, Marianthi, Corton, Marta, Van Schil, Kristof, Peelman, Frank, Cherry, Timothy, Rosseel, Toon, Verdin, Hannah, Derolez, Julien, Van Laethem, Thalia, Khan, Kamron N., McKibbin, Martin, Toomes, Carmel, Ali, Manir, Torella, Annalaura, Testa, Francesco, Jimenez, Belen, Simonelli, Francesca, De Zaeytijd, Julie, Van den Ende, Jenneke, Leroy, Bart P., Coppieters, Frauke, Ayuso, Carmen, Inglehearn, Chris F., Banfi, Sandro, De Baere, Elfride
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group US 2019
Matèries:
Correction
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6752296/
https://ncbi.nlm.nih.gov/pubmed/30607024
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41436-018-0392-y
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