Exome Sequencing Analysis in Severe, Early-Onset Chronic Obstructive Pulmonary Disease

Rationale: Genomic regions identified by genome-wide association studies explain only a small fraction of heritability for chronic obstructive pulmonary disease (COPD). Alpha-1 antitrypsin deficiency shows that rare coding variants of large effect also influence COPD susceptibility. We hypothesized...

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Vydáno v:Am J Respir Crit Care Med
Hlavní autoři: Qiao, Dandi, Lange, Christoph, Beaty, Terri H., Crapo, James D., Barnes, Kathleen C., Bamshad, Michael, Hersh, Craig P., Morrow, Jarrett, Pinto-Plata, Victor M., Marchetti, Nathaniel, Bueno, Raphael, Celli, Bartolome R., Criner, Gerald J., Silverman, Edwin K., Cho, Michael H.
Médium: Artigo
Jazyk:Inglês
Vydáno: American Thoracic Society 2016
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4910887/
https://ncbi.nlm.nih.gov/pubmed/26736064
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.201506-1223OC
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