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Cystic Fibrosis Mechanism and Treatment

Author(s): HHMI BioInteractive

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Summary:
This animation shows how mutations in an ion channel protein lead to the genetic disease cystic fibrosis. The animation also discusses how research on this protein has been used to develop treatments for the disease.

Licensed under CC Attribution-NonCommercial-NoDerivatives 4.0 International according to these terms

Version 1.0 - published on 01 Jul 2019 doi:10.25334/3RFD-6T62 - cite this

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