Exome Sequencing of Neonatal Blood Spots and the Identification of Genes Implicated in Bronchopulmonary Dysplasia

Rationale: Bronchopulmonary dysplasia (BPD), a prevalent severe lung disease of premature infants, has a strong genetic component. Large-scale genome-wide association studies for common variants have not revealed its genetic basis. Objectives: Given the historical high mortality rate of extremely pr...

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Vydáno v:Am J Respir Crit Care Med
Hlavní autoři: Li, Jingjing, Yu, Kun-Hsing, Oehlert, John, Jeliffe-Pawlowski, Laura L., Gould, Jeffrey B., Stevenson, David K., Snyder, Michael, Shaw, Gary M., O’Brodovich, Hugh M.
Médium: Artigo
Jazyk:Inglês
Vydáno: American Thoracic Society 2015
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4595691/
https://ncbi.nlm.nih.gov/pubmed/26030808
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.201501-0168OC
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