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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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| Hlavní autoři: | , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Group
2005
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| Témata: | |
| On-line přístup: | 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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