| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8751041 | Revue de Pneumologie Clinique | 2017 | 4 Pages |
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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Authors
M. Verduyn, M. Rigaud, C. Dromer,