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Raidt J, Krenz H, Tebbe J, et al. Limitations of nasal nitric oxide measurement for diagnosis of primary ciliary dyskinesia with normal ultrastructure. Ann Am Thorac Soc 19: 1275-1284, 2022.","DOI":"10.1513\/AnnalsATS.202106-728OC"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Knowles MR, Ostrowski LE, Leigh MW, et al. Mutations in <i>RSPH1<\/i> cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype. Am J Respir Crit Care Med 189: 707-717, 2014.","DOI":"10.1164\/rccm.201311-2047OC"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Shoemark A, Moya E, Hirst RA, et al. High prevalence of CCDC103 p.His154Pro mutation causing primary ciliary dyskinesia disrupts protein oligomerisation and is associated with normal diagnostic investigations. Thorax 73: 157-166, 2018.","DOI":"10.1136\/thoraxjnl-2017-209999"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Fassad MR, Shoemark A, Legendre M, et al. 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