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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Detalhes bibliográficos
Publicado no:Am J Respir Crit Care Med
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: American Thoracic Society 2017
Assuntos:
Original Articles
Acesso em linha: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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