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

PURPOSE: RAX2 encodes a homeobox-containing transcription factor, in which four monoallelic pathogenic variants have been described in autosomal dominant cone-dominated retinal disease. METHODS: Exome sequencing in a European cohort with inherited retinal disease (IRD) (n = 2086) was combined with p...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752271/
https://www.ncbi.nlm.nih.gov/pubmed/30377383
http://dx.doi.org/10.1038/s41436-018-0345-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752271/
https://www.ncbi.nlm.nih.gov/pubmed/30377383
http://dx.doi.org/10.1038/s41436-018-0345-5

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