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...

Полное описание

Сохранить в:
Библиографические подробности
Опубликовано в: :Am J Respir Crit Care Med
Главные авторы: 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.
Формат: Artigo
Язык:Inglês
Опубликовано: American Thoracic Society 2017
Предметы:
Original Articles
Online-ссылка: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
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы