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Editorial
. 2020 Mar;62(3):281-282.
doi: 10.1165/rcmb.2019-0316ED.

HY-DIN' in the Cilia: Discovery of Central Pair-related Mutations in Primary Ciliary Dyskinesia

Susan K Dutcher  1 , Steven L Brody  2
Affiliations
Editorial

HY-DIN' in the Cilia: Discovery of Central Pair-related Mutations in Primary Ciliary Dyskinesia

Susan K Dutcher et al. Am J Respir Cell Mol Biol. 2020 Mar.
No abstract available

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References

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    1. Dalrymple RA, Kenia P. European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia: a guideline review. Arch Dis Child Educ Pract Ed. 2019;104:265–269. - PubMed
    1. Shapiro AJ, Leigh MW. Value of transmission electron microscopy for primary ciliary dyskinesia diagnosis in the era of molecular medicine: genetic defects with normal and non-diagnostic ciliary ultrastructure. Ultrastruct Pathol. 2017;41:373–385. - PMC - PubMed
    1. Horani A, Ferkol TW. Advances in the genetics of primary ciliary dyskinesia: clinical implications. Chest. 2018;154:645–652. - PMC - PubMed
    1. Claes KB, De Leeneer K. Dealing with pseudogenes in molecular diagnostics in the next-generation sequencing era. Methods Mol Biol. 2014;1167:303–315. - PubMed

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