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Primary ciliary dyskinesia: From diagnosis to molecular mechanisms
Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disorder affecting motile cilia. This can lead to neonatal respiratory distress, early onset upper and lower airway infections, laterality abnormalities and sub- or infertility. Although disease progression shows large individual variabi...
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| 出版年: | J Pediatr Genet |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Georg Thieme Verlag KG
2014
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5020995/ https://ncbi.nlm.nih.gov/pubmed/27625868 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/PGE-14088 |
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