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Sep 6, 2022 (publication date) through Nov 24, 2024
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Zhang YY, Lou Y, Yan H, Tang H. CCNO mutation as a cause of primary ciliary dyskinesia: A case report. World J Clin Cases 2022; 10(25): 9148-9155 [PMID: 36157652 DOI: 10.12998/wjcc.v10.i25.9148] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v10/i25/9148.htm |
| Number | Citing Articles |
| 1 |
A. A. Novak, Yu. L. Mizernitskiy. Parallels between clinical and genetic characteristics in children with primary ciliary dyskinesia. PULMONOLOGIYA 2024; 34(2): 176 doi: 10.18093/0869-0189-2024-34-2-176-183
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| 2 |
Yifei Xu, Koki Ueda, Tomoki Nishikido, Tsubasa Matsumoto, Kazuhiko Takeuchi. Two Japanese Pediatric Patients With Primary Ciliary Dyskinesia Caused by Loss-of-Function Variants in the CCNO gene. Cureus 2024; doi: 10.7759/cureus.58854
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| 3 |
Lejun Tong, Li Li, Wenjian Wang, Jiehua Chen. Case Report: Primary ciliary dyskinesia due to CCNO mutations: a Chinese pediatric case series and literature review. Frontiers in Pediatrics 2024; 12 doi: 10.3389/fped.2024.1458660
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| 4 |
Ola Alhalabi, Atqah Abdulwahab, Merlin Thomas. The First Case of a Homozygous CCNO NM 021147.4 Mutation Associated With Primary Ciliary Dyskinesia in Two Indian Siblings. Cureus 2024; doi: 10.7759/cureus.52237
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| 5 |
Mehmet Halil Celiksoy, Işılay Turan, Alper Gezdirici, Ozgecan Kayalar, Çiğdem Aydoğmuş, Sezin Naiboglu. A novel homozygous frameshift CCNO variant presenting with primary ciliary dyskinesia and selective IgM deficiency. Pediatric Pulmonology 2023; 58(11): 3333 doi: 10.1002/ppul.26607
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