Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and Genotype

Rationale: In primary ciliary dyskinesia, factors leading to disease heterogeneity are poorly understood. Objectives: To describe early lung disease progression in primary ciliary dyskinesia and identify associations between ultrastructural defects and genotypes with clinical phenotype. Methods: Thi...

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發表在:Am J Respir Crit Care Med
Main Authors: Davis, Stephanie D., Rosenfeld, Margaret, Lee, Hye-Seung, Ferkol, Thomas W., Sagel, Scott D., Dell, Sharon D., Milla, Carlos, Pittman, Jessica E., Shapiro, Adam J., Sullivan, Kelli M., Nykamp, Keith R., Krischer, Jeffrey P., Zariwala, Maimoona A., Knowles, Michael R., Leigh, Margaret W.
格式: Artigo
語言:Inglês
出版: American Thoracic Society 2019
主題:
Original Articles
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6353004/
https://ncbi.nlm.nih.gov/pubmed/30067075
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.201803-0548OC
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