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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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| 出版年: | PLoS Genet |
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| 主要な著者: | , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Public Library of Science
2020
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| 主題: | |
| オンライン･アクセス: | 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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