Management of suspected monogenic lung fibrosis in a specialised centre

At least 10% of patients with interstitial lung disease present monogenic lung fibrosis suspected on familial aggregation of pulmonary fibrosis, specific syndromes or early age of diagnosis. Approximately 25% of families have an identified mutation in genes mostly involved in telomere homeostasis, a...

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Detalles Bibliográficos
Autores principales: Borie, Raphael, Kannengiesser, Caroline, Sicre de Fontbrune, Flore, Gouya, Laurent, Nathan, Nadia, Crestani, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2017
Materias:
Frontiers in Clinical Practice
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489110/
https://www.ncbi.nlm.nih.gov/pubmed/28446600
http://dx.doi.org/10.1183/16000617.0122-2016

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489110/
https://www.ncbi.nlm.nih.gov/pubmed/28446600
http://dx.doi.org/10.1183/16000617.0122-2016

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