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Mutation Screening in the miR-183/96/182 Cluster in Patients With Inherited Retinal Dystrophy
Inherited retinal dystrophy (IRD) is a heterogenous blinding eye disease and affects more than 200,000 Americans and millions worldwide. By far, 270 protein-coding genes have been identified to cause IRD when defective. However, only one microRNA (miRNA), miR-204, has been reported to be responsible...
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| 出版年: | Front Cell Dev Biol |
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| 主要な著者: | , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Frontiers Media S.A.
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7785829/ https://ncbi.nlm.nih.gov/pubmed/33425925 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcell.2020.619641 |
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