Genomic Fingerprint Associated with Familial Idiopathic Pulmonary Fibrosis: A Review

Idiopathic pulmonary fibrosis (IPF) is a severe interstitial lung disease; although the recent introduction of two anti-fibrosis drugs, pirfenidone and Nidanib, have resulted in a significant reduction in lung function decline, IPF is still not curable. Approximately 2-20% of patients with IPF have...

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Detalles Bibliográficos
Autores principales: Ding, Dongyan, Gao, Rong, Xue, Qianfei, Luan, Rumei, Yang, Junling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969503/
https://www.ncbi.nlm.nih.gov/pubmed/36860670
http://dx.doi.org/10.7150/ijms.80358

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969503/
https://www.ncbi.nlm.nih.gov/pubmed/36860670
http://dx.doi.org/10.7150/ijms.80358

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