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Primary Ciliary Dyskinesia: An Update on New Diagnostic Modalities and Review of the Literature
Primary ciliary dyskinesia (PCD) is a genetic condition affecting approximately 1 in 15,000–20,000 individuals, and the majority of cases exhibit an autosomal recessive inheritance pattern. However, genetic heterogenicity is seen in PCD and reflects the complexity of ciliary structure and biogenesis...
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| Autori principali: | , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Mary Ann Liebert, Inc.
2014
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4062113/ https://ncbi.nlm.nih.gov/pubmed/24963453 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/ped.2013.0314 |
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