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The Emerging Genetics of Primary Ciliary Dyskinesia
Primary ciliary dyskinesia (PCD) is an autosomal recessive, rare, genetically heterogeneous condition characterized by oto-sino-pulmonary disease together with situs abnormalities (Kartagener syndrome) owing to abnormal ciliary structure and function. Most patients are currently diagnosed with PCD b...
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| 主要な著者: | , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Thoracic Society
2011
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3209577/ https://ncbi.nlm.nih.gov/pubmed/21926394 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1513/pats.201103-023SD |
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