HY-DIN’ in the Cilia: Discovery of Central Pair–related Mutations in Primary Ciliary Dyskinesia
Author:
Affiliation:
1. Department of GeneticsWashington University School of MedicineSaint Louis, Missouriand
2. Department of MedicineWashington University School of MedicineSaint Louis, Missouri
Publisher
American Thoracic Society
Subject
Cell Biology,Clinical Biochemistry,Pulmonary and Respiratory Medicine,Molecular Biology
Link
https://www.atsjournals.org/doi/pdf/10.1165/rcmb.2019-0316ED
Reference13 articles.
1. Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline
2. European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia: a guideline review
3. 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
4. Advances in the Genetics of Primary Ciliary Dyskinesia
5. Dealing with Pseudogenes in Molecular Diagnostics in the Next-Generation Sequencing Era
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