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Ancestry and genetic associations with bronchopulmonary dysplasia in preterm infants
Bronchopulmonary dysplasia in premature infants is a common and often severe lung disease with long-term sequelae. A genetic component is suspected but not fully defined. We performed an ancestry and genome-wide association study to identify variants, genes, and pathways associated with survival wit...
Enregistré dans:
| Publié dans: | Am J Physiol Lung Cell Mol Physiol |
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| Auteurs principaux: | , , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
American Physiological Society
2018
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6295513/ https://ncbi.nlm.nih.gov/pubmed/30113228 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajplung.00073.2018 |
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