Genetic interaction between central pair apparatus genes CFAP221, CFAP54, and SPEF2 in mouse models of primary ciliary dyskinesia

Primary ciliary dyskinesia (PCD) is a genetically heterogeneous syndrome that results from defects in motile cilia. The ciliary axoneme has a 9 + 2 microtubule structure consisting of nine peripheral doublets surrounding a central pair apparatus (CPA), which plays a critical role in regulating prope...

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Detalles Bibliográficos
Autores principales: McKenzie, Casey W., Lee, Lance
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378221/
https://www.ncbi.nlm.nih.gov/pubmed/32704025
http://dx.doi.org/10.1038/s41598-020-69359-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378221/
https://www.ncbi.nlm.nih.gov/pubmed/32704025
http://dx.doi.org/10.1038/s41598-020-69359-3

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