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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Udgivet i: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
Format: Artigo
Sprog:Inglês
Udgivet: Public Library of Science 2020
Fag:
Research Article
Online adgang: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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