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Autor:
Fernando J. Martinez, Heather W. Stout-Delgado, Charles S. Dela Cruz, William Whalen, Bethany B. Moore, Jan Krumsiek, Soo Jung Cho, Augustine M.K. Choi, Mustafa Buyukozkan, Jong-Seok Moon
Publikováno v:
Thorax. 77(2)
Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal lung disease with unclear aetiology and poorly understood pathophysiology. Although plasma levels of circulating cell-free DNA (ccf-DNA) and metabolomic changes have been reported in IPF,