Mutation analysis in cystic fibrosis

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dc.contributor.authorGasparini, Paolo
dc.contributor.authorPignatti, P. F.
dc.contributor.authorNovelli, Giuseppe
dc.contributor.authorDallapiccola, B.
dc.contributor.authorNunes Martínez, Virginia
dc.contributor.authorCasals, T.
dc.contributor.authorEstivill, Xavier, 1955-
dc.contributor.authorFernández Muñoz, Esteve
dc.contributor.authorBalassopoulou, A.
dc.contributor.authorLoukopoulos, D.
dc.contributor.authorLavinha, J.
dc.contributor.authorSimova, L.
dc.contributor.authorKomel, R.
dc.date.accessioned2013-06-07T08:23:54Z
dc.date.available2013-06-07T08:23:54Z
dc.date.issued1990-07-05
dc.date.updated2013-06-07T08:23:54Z
dc.description.abstractThe 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...
dc.format.extent2 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec576706
dc.identifier.issn0028-4793
dc.identifier.urihttps://hdl.handle.net/2445/44105
dc.language.isoeng
dc.publisherMassachusetts Medical Society
dc.relation.isformatofReproducció del document publicat a: http://dx.doi.org/10.1056/NEJM199007053230114
dc.relation.ispartofNew England Journal of Medicine, 1990, vol. 323, num. 1, p. 62-63
dc.relation.urihttp://dx.doi.org/10.1056/NEJM199007053230114
dc.rights(c) Massachusetts Medical Society, 1990
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Ciències Fisiològiques)
dc.subject.classificationFibrosi quística
dc.subject.otherCystic fibrosis
dc.titleMutation analysis in cystic fibrosis
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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