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

• Hoofdauteurs: Francesco Chiani (Auteur), Tiziana Orsini (Auteur), Alessia Gambadoro (Auteur), Miriam Pasquini (Auteur), Sabrina Putti (Auteur), Maurizio Cirilli (Auteur), Olga Ermakova (Auteur), Glauco P. Tocchini-Valentini (Auteur)
• Formaat: Boek
• Gepubliceerd in: The Company of Biologists, 2019-08-01T00:00:00Z.
• Onderwerpen: article
• Online toegang: Connect to this object online.

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...