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Primary ciliary dyskinesia: mechanisms and management
Primary ciliary dyskinesia is a genetically heterogeneous disorder of motile cilia that is predominantly inherited in an autosomal-recessive fashion. It is associated with abnormal ciliary structure and/or function leading to chronic upper and lower respiratory tract infections, male infertility, an...
Sparad:
I publikationen: | Appl Clin Genet |
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Huvudupphovsmän: | , , , , |
Materialtyp: | Artigo |
Språk: | Inglês |
Publicerad: |
Dove Medical Press
2017
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Ämnen: | |
Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5614735/ https://ncbi.nlm.nih.gov/pubmed/29033599 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S127129 |
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