P085 &lt;break /&gt; The proteome signature of Idiopathic Pulmonary Fibrosis identifies distinct biological processes and molecular functions.

O’Dwyer, David N.; Norman, Katy C.; Xia, Meng; Murray, Susan; Grant, Ethan P.; White, Eric S.; Flaherty, Kevin R.; Martínez, Fernando J.; Arnold, Kelly B.; Moore, Bethany B.

doi:10.1093/qjmed/hcw127.021

QJM: An International Journal of Medicine

2016

DOI: 10.1093/qjmed/hcw127.021

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P085 <break /> The proteome signature of Idiopathic Pulmonary Fibrosis identifies distinct biological processes and molecular functions.

David N. O’Dwyer

Katy C. Norman

Meng Xia

et al.

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P085 <break /> The proteome signature of Idiopathic Pulmonary Fibrosis identifies distinct biological processes and molecular functions.

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