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National Emphysema Treatment Trial State of the Art: Genetics of Emphysema
Although a hereditary contribution to emphysema has been long suspected, severe α(1)-antitrypsin deficiency remains the only conclusively proven genetic risk factor for chronic obstructive pulmonary disease (COPD). Recently, genome-wide linkage analysis has led to the identification of two promising...
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| Autores principales: | , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
American Thoracic Society
2008
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2645324/ https://ncbi.nlm.nih.gov/pubmed/18453360 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1513/pats.200706-078ET |
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