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Cystic Fibrosis Mechanism and Treatment | HHMI BioInteractive Video
Mutations in the CFTR gene, which encodes a transmembrane ion channel, cause mucus buildup in the airways of patients with cystic fibrosis. This animation can be used to illustrate the connection between genotype and phenotype using a human disease example. It also demonstrates how knowledge about the genetic mutations responsible for a ...
324.6K viewsApr 19, 2018
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