Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/44105
Title: Mutation analysis in cystic fibrosis
Author: Gasparini, P.
Pignatti, P.F.
Novelli, G.
Dallapiccola, B.
Nunes Martínez, Virginia
Casals, T.
Estivill, Xavier, 1955-
Fernández, E.
Balassopoulou, A.
Loukopoulos, D.
Lavinha, J.
Simova, L.
Komel, R.
Keywords: Fibrosi quística
Cystic fibrosis
Issue Date: 5-Jul-1990
Publisher: Massachusetts Medical Society
Abstract: 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...
Note: Reproducció del document publicat a: http://dx.doi.org/10.1056/NEJM199007053230114
It is part of: New England Journal of Medicine, 1990, vol. 323, num. 1, p. 62-63
Related resource: http://dx.doi.org/10.1056/NEJM199007053230114
URI: http://hdl.handle.net/2445/44105
ISSN: 0028-4793
Appears in Collections:Articles publicats en revistes (Ciències Fisiològiques)

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