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Letters to the editor
Combined pulmonary fibrosis and emphysema syndrome associated with familial SFTPC mutation
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  1. Correspondence to Vincent Cottin, Hôpital Louis Pradel, Service de pneumologie, Lyon (Bron) Cedex 69677, France; vincent.cottin{at}chu-lyon.fr
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Citation

Cottin V, Reix P, Khouatra C, et al
Combined pulmonary fibrosis and emphysema syndrome associated with familial SFTPC mutation

Publication history

  • Accepted December 9, 2010
  • First published January 19, 2011.
Online issue publication 
September 01, 2022

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