Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis

C. Kannengiesser,R. Borie,C. Ménard,M. Réocreux,P. Nitschké,S. Gazal,H. Mal,C. Taillé,J. Cadranel,H. Nunes,D. Valeyre,J. Cordier,I. Callebaut,C. Boileau,V. Cottin,B. Grandchamp,P. Revy,B. Crestani

Published 2015 in European Respiratory Journal

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