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Clinical and Genetic Analysis of Children with Kartagener Syndrome
Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disorder characterized by dysfunction of motile cilia causing ineffective mucus clearance and organ laterality defects. In this study, two unrelated Portuguese children with strong PCD suspicion underwent extensive clinical and genetic a...
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| Pubblicato in: | Cells |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
MDPI
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6721662/ https://ncbi.nlm.nih.gov/pubmed/31443223 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells8080900 |
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