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Association of tumour necrosis factor alpha variants with the CF pulmonary phenotype

Background: The pulmonary phenotype in patients with cystic fibrosis (CF), even in those with the same CF transmembrane conductance regulator (CFTR) genotype, is variable and must therefore be influenced by secondary genetic factors as well as environmental factors. Possible candidate genes that mod...

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Detalhes bibliográficos
Main Authors: Yarden, J, Radojkovic, D, De Boeck, K, Macek, M, Zemkova, D, Vavrova, V, Vlietinck, R, Cassiman, J, Cuppens, H
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2005
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1747362/
https://ncbi.nlm.nih.gov/pubmed/15790988
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/thx.2004.025262
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