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Mills, Ross Jack
BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is one of a number of interstitial lung diseases (ILDs) that result in extensive and chronic pulmonary fibrosis. In IPF pathology, immunological dysfunction has been identified as a contributing factor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______463::964d76a3af98239b42d2d246659fb37c
http://hdl.handle.net/1842/29615
http://hdl.handle.net/1842/29615
