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Mutation analysis in cystic fibrosis
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The article by Lemna et al. (Feb. 1 issue)1 furthers the evaluation of the ΔF508 mutation, which is associated with some cases of cystic fibrosis. Although its real effect may be to help in documenting the substantial clinical variation that can occur among persons who possess the same small genetic deletion, the finding has encouraged calls for general screening...
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GASPARINI, Paolo, et al. Mutation analysis in cystic fibrosis. New England Journal of Medicine. 1990. Vol. 323, num. 1, pags. 62-63. ISSN 0028-4793. [consulted: 14 of June of 2026]. Available at: https://hdl.handle.net/2445/44105