An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis

Rationale: Idiopathic pulmonary fibrosis (IPF) is an increasingly recognized, often fatal lung disease of unknown etiology. Objectives: The aim of this study was to use whole-exome sequencing to improve understanding of the genetic architecture of pulmonary fibrosis. Methods: We performed a case–con...

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Detaylı Bibliyografya
Yayımlandı:Am J Respir Crit Care Med
Asıl Yazarlar: Petrovski, Slavé, Todd, Jamie L., Durheim, Michael T., Wang, Quanli, Chien, Jason W., Kelly, Fran L., Frankel, Courtney, Mebane, Caroline M., Ren, Zhong, Bridgers, Joshua, Urban, Thomas J., Malone, Colin D., Finlen Copeland, Ashley, Brinkley, Christie, Allen, Andrew S., O’Riordan, Thomas, McHutchison, John G., Palmer, Scott M., Goldstein, David B.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Thoracic Society 2017
Konular:
Original Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5519963/
https://ncbi.nlm.nih.gov/pubmed/28099038
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.201610-2088OC
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