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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 t
Externí odkaz:
https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.743707
