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Association of the MUC5B promoter polymorphism with idiopathic pulmonary fibrosis in a lebanese cohort

Background and objectiveIdiopathic Pulmonary Fibrosis (IPF) is an interstitial lung disease that causes irreversible alterations in the architecture of the lung parenchyma, leading to impaired ventilation. Both environmental factors and genetic predisposition play significant roles in the developmen...

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Bibliografische Detailangaben
Hauptverfasser: Antoine Mouawad, Eliane Chouery, Alain Chebly, Nabiha Salem, Sandra Corbani, Maissa Safieddine, Georges Dabar
Format: Artigo
Sprache:Inglês
Veröffentlicht: Frontiers Media S.A. 2025-06-01
Schriftenreihe:Frontiers in Genetics
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Online-Zugang:https://www.frontiersin.org/articles/10.3389/fgene.2025.1544864/full
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