Re: zebrafish ciliopathy screen plus human mutational analysis identifies C21orf59 and CCDC65 defects as causing primary ciliary dyskinesia
- PMID: 24745522
- DOI: 10.1016/j.juro.2014.02.023
Re: zebrafish ciliopathy screen plus human mutational analysis identifies C21orf59 and CCDC65 defects as causing primary ciliary dyskinesia
Comment on
-
Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.Am J Hum Genet. 2013 Oct 3;93(4):672-86. doi: 10.1016/j.ajhg.2013.08.015. Am J Hum Genet. 2013. PMID: 24094744 Free PMC article.
Similar articles
-
Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.Am J Hum Genet. 2013 Oct 3;93(4):672-86. doi: 10.1016/j.ajhg.2013.08.015. Am J Hum Genet. 2013. PMID: 24094744 Free PMC article.
-
Exclusion of chromosome 7 for Kartagener syndrome but suggestion of linkage in families with other forms of primary ciliary dyskinesia.Am J Hum Genet. 1999 Jan;64(1):313-8. doi: 10.1086/302203. Am J Hum Genet. 1999. PMID: 9915976 Free PMC article. No abstract available.
-
Mechanisms of mammalian ciliary motility: Insights from primary ciliary dyskinesia genetics.Gene. 2011 Mar 1;473(2):57-66. doi: 10.1016/j.gene.2010.11.006. Epub 2010 Nov 25. Gene. 2011. PMID: 21111794 Review.
-
Novel deletion mutations of the PIH1D3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with Kartagener's syndrome.Asian J Androl. 2021 May-Jun;23(3):330-332. doi: 10.4103/aja.aja_43_20. Asian J Androl. 2021. PMID: 33106461 Free PMC article. No abstract available.
-
Ciliary dyskinesia in the nose and paranasal sinuses.Acta Otorhinolaryngol Belg. 1997;51(4):353-66. Acta Otorhinolaryngol Belg. 1997. PMID: 9444381 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources