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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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Bibliografski detalji
Izdano u:Am J Respir Crit Care Med
Glavni autori: 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.
Format: Artigo
Jezik:Inglês
Izdano: American Thoracic Society 2019
Teme:
Online pristup: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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