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Clinical and Genetic Aspects of Primary Ciliary Dyskinesia / Kartagener Syndrome
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder of motile cilia. Most of the disease-causing mutations identified to date involve the heavy (DNAH5) or intermediate (DNAI1) chain dynein genes in ciliary outer dynein arms, although a few mutations have been noted in other gene...
Bewaard in:
| Hoofdauteurs: | , , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2009
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3739704/ https://ncbi.nlm.nih.gov/pubmed/19606528 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/GIM.0b013e3181a53562 |
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