New Cystic Fibrosis Treatment a GameChanger SciShow News

The transcript discusses the discovery of the CFTR gene responsible for cystic fibrosis and the development of Trikafta, a drug that significantly improves lung function for many patients. Despite its promise, Trikafta is expensive and only effective for certain mutations, highlighting the need for broader treatments. The transcript also covers the history of cystic fibrosis, the challenges of treating it, and the future direction of research aimed at finding a universal cure.

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