A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice
Primary ciliary dyskinesia (PCD) is a human condition of dysfunctional motile cilia characterized by recurrent lung infection, infertility, organ laterality defects and partially penetrant hydrocephalus. We recovered a mouse mutant from a forward genetic screen that developed many of the hallmark ph...
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| Main Authors: | , , , , |
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| Format: | Book |
| Published: |
The Company of Biologists,
2020-10-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |