Clinical phenotype of cystic fibrosis patients with the G551D mutation


Autoria(s): Comer, D.M.; Ennis, Madeleine; McDowell, C.; Beattie, D.; Rendall, J.; Hall, V.; Elborn, Joseph
Data(s)

01/11/2009

Resumo

Background: Data on whether the phenotype of cystic fibrosis (CF) patients with compound heterozygocity for G551D (Gly551Asp) differs from patients with F508del (Phe508del) homozygous mutations is divergent.

Identificador

http://pure.qub.ac.uk/portal/en/publications/clinical-phenotype-of-cystic-fibrosis-patients-with-the-g551d-mutation(18118c8f-6212-472c-9b69-a238233439e5).html

http://dx.doi.org/10.1093/qjmed/hcp120

http://www.scopus.com/inward/record.url?scp=77249140148&partnerID=8YFLogxK

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Comer , D M , Ennis , M , McDowell , C , Beattie , D , Rendall , J , Hall , V & Elborn , J 2009 , ' Clinical phenotype of cystic fibrosis patients with the G551D mutation ' QJM-AN INTERNATIONAL JOURNAL OF MEDICINE , vol 102 , no. 11 , pp. 793-798 . DOI: 10.1093/qjmed/hcp120

Palavras-Chave #/dk/atira/pure/subjectarea/asjc/2700 #Medicine(all)
Tipo

article