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Reptin/Ruvbl2 is a Lrrc6/Seahorse interactor essential for cilia motility
Primary ciliary dyskinesia (PCD) is an autosomal recessive disease caused by defective cilia motility. The identified PCD genes account for about half of PCD incidences and the underlying mechanisms remain poorly understood. We demonstrate that Reptin/Ruvbl2, a protein known to be involved in epigen...
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| Main Authors: | , , , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
National Academy of Sciences
2013
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3732945/ https://ncbi.nlm.nih.gov/pubmed/23858445 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1300968110 |
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