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[A rare familial form of idiopathic pulmonary fibrosis with Poly(A)-specific ribonuclease (PARN) mutation].

Authors
  • Verduyn, M1
  • Rigaud, M2
  • Dromer, C2
  • 1 Service des maladies respiratoires, CHU de Bordeaux, avenue Magellan, 33600 Pessac, France. Electronic address: [email protected] , (France)
  • 2 Service des maladies respiratoires, CHU de Bordeaux, avenue Magellan, 33600 Pessac, France. , (France)
Type
Published Article
Journal
Revue de Pneumologie Clinique
Publisher
Elsevier
Publication Date
Oct 01, 2017
Volume
73
Issue
5
Pages
272–275
Identifiers
DOI: 10.1016/j.pneumo.2017.07.004
PMID: 29055513
Source
Medline
Keywords
License
Unknown

Abstract

New techniques of DNA sequences allow to discover genetics mutations involved in familial pulmonary fibrosis. Among them, the PARN (Poly[A]-specific ribonuclease) mutation. Herein, we report the case of one patient who has pulmonary fibrosis with PARN mutation and the experience of our patient care.

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