HIT-CF, a European Union-funded research project, is working to provide personalized disease-modifying treatments to cystic fibrosis (CF) patients with rare CFTR mutations who lack effective treatment options. ӗe hope that within five years, these ż/p>
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raleighfir1973 April 10, 2022Software
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https://hub.page/physical-disorders/personalized-medicines-for-rare-mutations-are-focus-of-hitcf-in-eu