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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Detalhes bibliográficos
Publicado no:PLoS Genet
Main Authors: 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
Idioma:Inglês
Publicado em: Public Library of Science 2020
Assuntos:
Research Article
Acesso em linha: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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