Mutation analysis in cystic fibrosis


Autoria(s): 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.
Contribuinte(s)

Universitat de Barcelona

Resumo

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...

Identificador

http://hdl.handle.net/2445/44105

Idioma(s)

eng

Publicador

Massachusetts Medical Society

Direitos

(c) Massachusetts Medical Society, 1990

info:eu-repo/semantics/openAccess

Palavras-Chave #Fibrosi quística #Cystic fibrosis
Tipo

info:eu-repo/semantics/article

info:eu-repo/semantics/publishedVersion