What progress is being made for people with rare CF mutations who currently can’t benefit from any modulator therapy? Projects like HIT-CF are focussing on this group to ensure they are not left behind in the development of new treatments. You can hear more about their work here: https://bit.ly/2JaFKMl We are also holding a CF Live event next Wednesday to talk about clinical trials and why they continue to be important for the #Future4CF. Join us to find out more by signing up here: https://bit.
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Theratyping, or the process of matching medications with mutations, is enabling more people with cystic fibrosis who have rare mutations to benefit from CFTR modulators. Watch this video to learn more about the importance of theratyping and see the impact it can have on people’s lives. | Cystic Fibrosis Foundation
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Answered: The mutations found in the CF gene that result in cystic fibrosis are recessive because.. (Justify your answer) a) CF is fatal and if the alleles that caused… | bartleby
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