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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...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Appl Clin Genet
Prif Awduron: Damseh, Nadirah, Quercia, Nada, Rumman, Nisreen, Dell, Sharon D, Kim, Raymond H
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Dove Medical Press 2017
Pynciau:
Mynediad Ar-lein: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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