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Heterozygosity for E292V in ABCA3, lung function and COPD in 64,000 individuals
BACKGROUND: Mutations in ATP-binding-cassette-member A3 (ABCA3) are related to severe chronic lung disease in neonates and children, but frequency of chronic lung disease due to ABCA3 mutations in the general population is unknown. We tested the hypothesis that individuals heterozygous for ABCA3 mut...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2012
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514156/ https://www.ncbi.nlm.nih.gov/pubmed/22866751 http://dx.doi.org/10.1186/1465-9921-13-67 |