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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Dades bibliogràfiques
Publicat a:PLoS Genet
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2020
Matèries:
Research Article
Accés en línia: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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