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

Eur Respir J. 2020 Apr 9;55(4):1901952. doi: 10.1183/13993003.01952-2019. Print 2020 Apr.

¹ National 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 vincent.cottin@chu-lyon.fr.
² National 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.
³ Dept of Pathology, Groupement Hospitalier Est, Hospices Civils de Lyon, Claude Bernard University Lyon 1, Lyon, France.
⁴ CHU Reims, Hôpital Maison Blanche, Pôle de Biologie, Service de Génétique, Reims, France.
⁵ Dept of Radiology, Louis Pradel Hospital, Hospices Civils de Lyon, Lyon, France.
⁶ Dept of Respiratory Medicine, Croix Rousse Hospital, Hospices Civils de Lyon, Lyon, France.

No abstract available

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