Recurring large deletion in DRC1 ( CCDC164 ) identified as causing primary ciliary dyskinesia in two Asian patients

Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline

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A targeted next-generation sequencing panel reveals novel mutations in Japanese patients with primary ciliary dyskinesia

(2018) Kazuhiko Takeuchi et al.   AURIS NASUS LARYNX

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

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The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans

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Genetic predisposition to diffuse panbronchiolitis

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