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Functional loss of Ccdc151 leads to hydrocephalus in a mouse model of primary ciliary dyskinesia
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder affecting normal structure and function of motile cilia, phenotypically manifested as chronic respiratory infections, laterality defects and infertility. Autosomal recessive mutations in genes encoding for different components...
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| Publié dans: | Dis Model Mech |
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| Auteurs principaux: | , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
The Company of Biologists Ltd
2019
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6737950/ https://ncbi.nlm.nih.gov/pubmed/31383820 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.038489 |
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