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Nitric oxide synthase 1 as a potential modifier gene of decline in lung function in patients with cystic fibrosis
Methods: Dinucleotide GT repeat polymorphism was studied in the 5' untranslated region of the NOS1 gene, immediately upstream from the transcription initiation site, in 59 patients with CF and 59 healthy controls. Results: Nineteen alleles of the NOS1 gene were identified according to the numbe...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Group
2004
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1746921/ https://ncbi.nlm.nih.gov/pubmed/14760158 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/thorax.2003.006718 |
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