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Prolidase deficiency: a new genetic cause of combined pulmonary fibrosis and emphysema syndrome in the adult

Vincent Cottin, Mouhamad Nasser, Julie Traclet, Lara Chalabreysse, Anne-Sophie Lèbre, Salim Si-Mohamed, François Philit, Françoise Thivolet-Béjui
European Respiratory Journal 2020; DOI: 10.1183/13993003.01952-2019
Vincent Cottin
1National Coordinating Reference Centre for Rare Pulmonary Diseases, Louis Pradel Hospital, Hospices Civils de Lyon, UMR 754, Claude Bernard University Lyon 1, member of OrphaLung, RespiFil, and ERN-LUNG, Lyon, France
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Mouhamad Nasser
1National Coordinating Reference Centre for Rare Pulmonary Diseases, Louis Pradel Hospital, Hospices Civils de Lyon, UMR 754, Claude Bernard University Lyon 1, member of OrphaLung, RespiFil, and ERN-LUNG, Lyon, France
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Julie Traclet
1National Coordinating Reference Centre for Rare Pulmonary Diseases, Louis Pradel Hospital, Hospices Civils de Lyon, UMR 754, Claude Bernard University Lyon 1, member of OrphaLung, RespiFil, and ERN-LUNG, Lyon, France
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Lara Chalabreysse
2Department of pathology, Groupement hospitalier Est, Hospices Civils de Lyon, Claude Bernard University Lyon 1, Lyon, France
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Anne-Sophie Lèbre
3CHU Reims, Hôpital Maison Blanche, Pôle de Biologie, Service de Génétique, Reims, France
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Salim Si-Mohamed
4Department of radiology, Louis Pradel Hospital, Hospices Civils de Lyon, Lyon, France
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François Philit
5Department of respiratory medicine, Croix Rousse Hospital, Hospices Civils de Lyon, Lyon, France
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Françoise Thivolet-Béjui
2Department of pathology, Groupement hospitalier Est, Hospices Civils de Lyon, Claude Bernard University Lyon 1, Lyon, France
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Article Information

DOI 
https://doi.org/10.1183/13993003.01952-2019
PubMed 
31980489

Published By 
European Respiratory Society
Print ISSN 
0903-1936
Online ISSN 
1399-3003
History 
  • Received October 10, 2019
  • Accepted December 19, 2019
  • Published online January 24, 2020.

Article Versions

  • You are currently viewing a previous version of this article (January 24, 2020 - 03:56).
  • View the most recent version of this article
Copyright & Usage 
Copyright ©ERS 2020

Author Information

  1. Vincent Cottin1,
  2. Mouhamad Nasser1,
  3. Julie Traclet1,
  4. Lara Chalabreysse2,
  5. Anne-Sophie Lèbre3,
  6. Salim Si-Mohamed4,
  7. François Philit5 and
  8. Françoise Thivolet-Béjui2
  1. 1National Coordinating Reference Centre for Rare Pulmonary Diseases, Louis Pradel Hospital, Hospices Civils de Lyon, UMR 754, Claude Bernard University Lyon 1, member of OrphaLung, RespiFil, and ERN-LUNG, Lyon, France
  2. 2Department of pathology, Groupement hospitalier Est, Hospices Civils de Lyon, Claude Bernard University Lyon 1, Lyon, France
  3. 3CHU Reims, Hôpital Maison Blanche, Pôle de Biologie, Service de Génétique, Reims, France
  4. 4Department of radiology, Louis Pradel Hospital, Hospices Civils de Lyon, Lyon, France
  5. 5Department of respiratory medicine, Croix Rousse Hospital, Hospices Civils de Lyon, Lyon, France
  1. Vincent Cottin, Service de pneumologie, Hôpital Louis Pradel, 28 avenue Doyen Lepine, F-69677 Lyon Cedex, France. E-mail: vincent.cottin{at}chu-lyon.fr
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Prolidase deficiency: a new genetic cause of combined pulmonary fibrosis and emphysema syndrome in the adult
Vincent Cottin, Mouhamad Nasser, Julie Traclet, Lara Chalabreysse, Anne-Sophie Lèbre, Salim Si-Mohamed, François Philit, Françoise Thivolet-Béjui
European Respiratory Journal Jan 2020, 1901952; DOI: 10.1183/13993003.01952-2019

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Prolidase deficiency: a new genetic cause of combined pulmonary fibrosis and emphysema syndrome in the adult
Vincent Cottin, Mouhamad Nasser, Julie Traclet, Lara Chalabreysse, Anne-Sophie Lèbre, Salim Si-Mohamed, François Philit, Françoise Thivolet-Béjui
European Respiratory Journal Jan 2020, 1901952; DOI: 10.1183/13993003.01952-2019
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