A putative silencer variant in a spontaneous canine model of retinitis pigmentosa

Retinitis pigmentosa (RP) is the leading cause of blindness with nearly two million people affected worldwide. Many genes have been implicated in RP, yet in 30–80% of the RP patients the genetic cause remains unknown. A similar phenotype, progressive retinal atrophy (PRA), affects many dog breeds in...

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Publicado en:PLoS Genet
Autores principales: Kaukonen, Maria, Quintero, Ileana B., Mukarram, Abdul Kadir, Hytönen, Marjo K., Holopainen, Saila, Wickström, Kaisa, Kyöstilä, Kaisa, Arumilli, Meharji, Jalomäki, Sari, Daub, Carsten O., Kere, Juha, Lohi, Hannes
Formato: Artigo
Lenguaje:Inglês
Publicado: Public Library of Science 2020
Materias:
Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC7082071/
https://ncbi.nlm.nih.gov/pubmed/32150541
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1008659
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