CCNO mutation as a cause of primary ciliary dyskinesia: A case report
Summary
The results showed that CCNO is an important cause of PCD. More mutant genes that may contribute to genetically diverse disorders like PCD have been discovered as sequencing technology has advanced. Furthermore, the increase of genetic information makes it easier to diagnose uncommon diseases in clinical practice. ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved.
| Authors | Zhang YY, Lou Y, Yan H, Tang H |
|---|---|
| Journal | World journal of clinical cases |
| Publication Date | 2022 Sep 6;10(25):9148-9155 |
| PubMed | 36157652 |
| PubMed Central | PMC9477031 |
| DOI | 10.12998/wjcc.v10.i25.9148 |