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

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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Main Authors: Francesco Chiani (Author), Tiziana Orsini (Author), Alessia Gambadoro (Author), Miriam Pasquini (Author), Sabrina Putti (Author), Maurizio Cirilli (Author), Olga Ermakova (Author), Glauco P. Tocchini-Valentini (Author)
Format: Book
Published: The Company of Biologists, 2019-08-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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