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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Detalhes bibliográficos
Publicado no: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.
Formato: Artigo
Idioma:Inglês
Publicado em: American Thoracic Society 2019
Assuntos:
Original Articles
Acesso em linha: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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