Functional loss of Ccdc151 leads to hydrocephalus in a mouse model of primary ciliary dyskinesia

Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder affecting normal structure and function of motile cilia, phenotypically manifested as chronic respiratory infections, laterality defects and infertility. Autosomal recessive mutations in genes encoding for different components...

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Detalles Bibliográficos
Autores principales: Chiani, Francesco, Orsini, Tiziana, Gambadoro, Alessia, Pasquini, Miriam, Putti, Sabrina, Cirilli, Maurizio, Ermakova, Olga, Tocchini-Valentini, Glauco P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737950/
https://www.ncbi.nlm.nih.gov/pubmed/31383820
http://dx.doi.org/10.1242/dmm.038489

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737950/
https://www.ncbi.nlm.nih.gov/pubmed/31383820
http://dx.doi.org/10.1242/dmm.038489

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